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@Pushpajhaaarti 2 күн бұрын
Kya same exam me aaayega
@VenusAcademy Күн бұрын
@@Pushpajhaaarti Yes madam, you will get same type of questions in IC38 exam
@zaidft4819 2 күн бұрын
Give answer
@VenusAcademy Күн бұрын
Option C
@VenusAcademy 5 күн бұрын
💁🏻𝗗𝗼𝘄𝗻𝗹𝗼𝗮𝗱 𝟭𝟬 𝐩𝐫𝐞𝐯𝐢𝐨𝐮𝐬 𝐲𝐞𝐚𝐫 𝐐𝐮𝐞𝐬𝐭𝐢𝐨𝐧 𝐏𝐚𝐩𝐞𝐫 𝐰𝐢𝐭𝐡 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧 | 𝗖𝗦𝗜𝗥-𝗡𝗘𝗧 | 𝗜𝗜𝗧 𝗝𝗔𝗠 | 𝗚𝗔𝗧𝗘👉 sites.google.com/site/venuschemistryacademy/exams/csir-ugc-net 👉 IIT JAM - 2018 Chemistry - kzbin.info/www/bejne/imOWpZ2QhJd7mpo PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLScRnQVr1GP8W0xs3zH4yFkRwI3S0n9QO8fliAxKDtCU6vyU6w/viewform 👉 IIT JAM - 2019 Chemistry - kzbin.info/www/bejne/fqKQhmONic-lqdE PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfqV4b9Yp67rq0Ce9I6uSzNLlGMXZ1ByjGfatMsS-f5IjILTw/viewform?usp=send_form 👉 IIT JAM - 2020 Chemistry - kzbin.info/www/bejne/p4bYq4F-lJucn9U PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfDrPk9QsBorTT-1Vgn16IWUnHkQhdf4LOcvbK-cWmuXrp_kw/viewform 👉 IIT JAM - 2021 Chemistry - kzbin.info/www/bejne/mp3UnJmwrslgoqs PDF Download with solutions: drive.google.com/file/d/1_loPCMISBkOhThsn4gVOpHNkm5LyHhdx/view?usp=sharingkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.pngkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.png 👉 IIT JAM - 2022 Chemistry video solutions: kzbin.info/www/bejne/hWbPhaxve5d6nrM IIT JAM - 2022 Chemistry PDF with solutions: drive.google.com/file/d/1E20zu3ZJTQgy-RgYqo_mHBGbJZmI9QDI/view?usp=sharing 👉 IIT JAM - 2023 Chemistry videos link: kzbin.info/www/bejne/aafWpqWZbNeIga8 PDF download free:drive.google.com/file/d/1471xnQsPLKhxe5kCyegoZ6ryemNxGxeR/view?usp=sharing #jam2025 #JAMCHEMISTRY2025 #iit #chemistry #namereaction #coupling #jchemistry #physicswallah #venusacademy The Joint Admission Test for Masters (JAM) has set the benchmark for undergraduate science education in the country for the past two decades. This prestigious exam paves the way for students to gain admission to top-tier postgraduate programs, solidifying science as a stellar career choice nationwide. Our programs offer world-class education in various disciplines, designed to cultivate academic excellence and a fulfilling professional life. What does JAM offer? JAM is not just an exam-it's a gateway to premier institutes offering high-quality postgraduate education. The interdisciplinary nature of the curriculum empowers students to translate scientific knowledge into real-world applications. These opportunities are open to all eligible students, regardless of nationality, with English as the medium of instruction. With a JAM score, you can pursue a range of advanced degrees, including: M.Sc. M.Sc. (Tech.) MS (Research) M.Sc. - M.Tech. Dual Degree Joint M.Sc. - Ph.D. M.Sc. - Ph.D. Dual Degree How Admissions Work Admissions through JAM 2025 are categorized into: Admitting Institutes: Coordinated by the JAM 2025 Organizing Institute. Result Sharing Institutes: Candidates must approach these institutes directly after qualifying. JAM 2025 Organizing Institute will coordinate the admission process of only the Admitting Institutes and the candidates can apply for Admission after qualifying the JAM 2025 examination. For admissions to Result Sharing Institutes qualifying candidates have to directly approach the respective Institute / admission body. In all matters concerning JAM 2025, the decision of the Organizing Institute, JAM 2025 will be final and binding on all the applicants #csir #gate #iit #jam #chemistry #physics #maths #clemenson #favorskii #rearrangement #name reactions #Grignard #cannizzaro #organicchemistry #coupling #jointadmissiontestformasters #masters #entranceexam #chemistry #jchemistry #byjus #vedantu #physicswallah #chemistrywallah #mathswallah #previousyearpaper
@AsheeshYadav-u5b 9 күн бұрын
Sir make all regent reaction workup handling please very helpful nice
@VenusAcademy 6 күн бұрын
Thank you Yadav ji, Please watch other reagents videos of 1. Sodium metal How to Cut Use and Quench/Clean/Destroy?? || Potassium metal? | Lab - 1.1 kzbin.info/www/bejne/nKKqo3xqj9h8ns0 2. DIBALH, LAH, NaH Metal Hydrides - HOW TO USE AND QUENCH LABORATORY SAFETY TRICKS || Lab - 1.2: kzbin.info/www/bejne/bKTCpGZsZ6qdhdEsi=NCgSuU1MS1mCda-5 3. Palladium on Carbon (Pd/C), Raney Ni - HOW TO USE AND QUENCH LABORATORY SAFETY TRICKS || Lab - 1.3:kzbin.info/www/bejne/haGwm3mMjbN1gLs Wish you all the best.
@AsheeshYadav-u5b 6 күн бұрын
@VenusAcademy please sir all reagent quenching handling and workup videos
@pallavichoudhary9184 12 күн бұрын
Good afternoon sir, Yesterday I was having my IRDA exam,so I saw your videos n I scored 32 out of 50. So thank you so much sir🙏
@VenusAcademy 10 күн бұрын
@@pallavichoudhary9184 Congratulations Madam, wish you all the Best 🙏
@ashwini9306 16 күн бұрын
I have exam tomorrow hope i will passed.....i will comment tomorrow about my results 🎉
@VenusAcademy 10 күн бұрын
@@ashwini9306 Wish you all the Best 🙏
@sudeshangre 16 күн бұрын
Almost all the syllabus is covered in this video. It helps people to get the exam passed, Thanks.
@VenusAcademy 10 күн бұрын
@@sudeshangre Thank you ji, Wish you all the best 🙏
@ravichandran-hy7ei 18 күн бұрын
Super sir
@VenusAcademy 10 күн бұрын
@@ravichandran-hy7ei Thank you Sir, wish you all the Best 🙏
@krishnamraju1826 18 күн бұрын
Hello sir please telugu
@VenusAcademy 10 күн бұрын
Madam As Time permits then I will make in Telugu also. Thank you 🙏
@mariaaugustin2718 18 күн бұрын
Kindly give us questions relevant for the year 2024 pm scheme sir
@VenusAcademy 10 күн бұрын
@@mariaaugustin2718 please follow other videos also..
@mariaaugustin2718 10 күн бұрын
Anyways thank you sir for your video I passed the exam scored 28 points
@VenusAcademy 9 күн бұрын
@@mariaaugustin2718 Congratulation Maria ji, wish you all the best.
@dhanalakshmid4280 23 күн бұрын
And how we prepare for exam
@dhanalakshmid4280 23 күн бұрын
Now govt conduct lic bhim saki yojana for womens for 10th pass plz vedio for this sceem
@VenusAcademy 21 күн бұрын
Yes madam, as time permits, I will make a video on Bhim Saki Yojana. Thank you, wish you all the best.
@dhanalakshmid4280 19 күн бұрын
Now I applied for beem saki yojana sceem so plz upload vedio what we prepare for exm
@dhanalakshmid4280 23 күн бұрын
Hi sir i am new subscriber
@VenusAcademy 21 күн бұрын
Thank you madam, wish you all the best.
@VenusAcademy 29 күн бұрын
Reformatsky Reaction: Overview The Reformatsky reaction is a chemical reaction that involves the formation of a β-hydroxy ester from an aldehyde or ketone and an α-bromo ester in the presence of zinc metal. General Reaction RCHO + BrCH₂COOR' + Zn → RCH(OH)CH₂COOR' Mechanism 1. Formation of a zinc-carbonyl complex. 2. Nucleophilic attack by the α-bromo ester on the carbonyl group. 3. Formation of a zinc alkoxide intermediate. 4. Protonation of the intermediate to form the β-hydroxy ester. Conditions 1. Zinc metal (Zn). 2. α-Bromo ester. 3. Aldehyde or ketone. 4. Solvent (e.g., diethyl ether, tetrahydrofuran). 5. Temperature (0°C to 50°C). Examples 1. Benzaldehyde + α-Bromo propionate → 3-Hydroxy-3-phenylpropanoate. 2. Acetophenone + α-Bromo acetate → 2-Hydroxy-2-phenylacetate. Advantages 1. Forms β-hydroxy esters, useful intermediates in organic synthesis. 2. Mild conditions. 3. Good yields. Limitations 1. Limited scope for certain aldehydes and ketones. 2. Requires zinc metal. 3. Can be slow. Variations 1. Modified Reformatsky reaction using ultrasound or microwave irradiation. 2. Asymmetric Reformatsky reaction using chiral catalysts. Related Reactions 1. Claisen condensation. 2. Aldol reaction. 3. Michael addition. Applications 1. Organic synthesis. 2. Pharmaceutical chemistry. 3. Natural product synthesis.🎉😢😮😂❤
@raoaiim6563 Ай бұрын
Bgm oh we can't listen ur voice sir
@VenusAcademy Ай бұрын
@@raoaiim6563 please watch other videos with clear voice In this Video you have Important question answers from Health Insurance section as below: Section - II: HEALTH INSURANCE (5 chapters) d. Chapter - 6: Introduction to Health Insurance Chapter - 7: Insurance Documentation Chapter-8: Health Insurance Products Chapter-9: Health Insurance Underwriting Chapter-10: Health Insurance Claims kzbin.info/www/bejne/Y2XHiGBqgcath7c ------------- 🙏 Please 👉SUBSCRIBE FREE 👍 & 🔔 100% Pass Guarantee online trainer Dr M V Chary ---------------------------- #ic38 #insurance #irda ________________ Dear Friends IC 38 IRDAI Insurance Agent Exam is of 3 types A. LIFE INSURANCE Agent Exam B. NON LIFE (GENERAL/MOTOR) INSURANCE Agent Exam C. HEALTH INSURANCE Agent Exam As per new syllabus of these 3 types I have given links to each type of exam please follow them as per the syllabus. ALL THE BEST “Explore the Box to THINK OUTSIDE THE BOX” __________ A. LIFE INSURANCE IC 38 IRDAI Agent Exam New Syllabus: Total 21 chapters divided into 3 sections:- Section-I: Common chapters (5 chapters) Section-II: Life insurance (11 chapters) Section-III: Health Insurance (5 chapters) as below: ---------------- I. Section- I : COMMON CHAPTERS (5 chapters) a. Chapter - 1: Introduction to Insurance kzbin.info/www/bejne/mpypgneMfZaCY8k b. Chapter - 2 Customer Service Chapter - 3: Grievance Redressal Mechanism kzbin.info/www/bejne/b3apfmV8ZdJ1bpI c. Chapter - 4: Regulatory aspects of Insurance Agents Chapter - 5: Legal Principle of an Insurance Contract kzbin.info/www/bejne/ppjZlK16nph9fcU ------- II. Section - II: LIFE INSURANCE (11 chapters) d. Chapter - 6: What Life Insurance Involves Chapter- 7: Financial Planning Chapter - 8: Life Insurance Products - I Chapter - 9: Life Insurance Products - II kzbin.info/www/bejne/gKTWkqOId7FshtU e. Chapter 10: Applications of Life Insurance Chapter 11: Pricing and Valuation in Life Insurance kzbin.info/www/bejne/sKW6mGhnnLdkoLc f. Chapter 12: Documentation - Proposal Stage Chapter 13: Documentation - Policy Condition 1 Chapter 14: Documentation - Policy Condition 2 kzbin.info/www/bejne/pKfbeoBveN1-atk g. Chapter 15: Underwriting Chapter 16: Payments under a Life Insurance Policy kzbin.info/www/bejne/npy1m4mtl9h-m80 III. Section - III: HEALTH INSURANCE (5 chapters) h. Chapter - 17: Introduction to Health Insurance Chapter - 18: Insurance Documentation Chapter-19: Health Insurance Products Chapter-20: Health Insurance Underwriting Chapter-21: Health Insurance Claims kzbin.info/www/bejne/Y2XHiGBqgcath7c ____________ B. GENERAL (MOTOR/NON LIFE) INSURANCE Agent Exam IC 38 IRDAI New Syllabus: Total 16 chapters divided into Three Sections Section-I: Common chapters (5 chapters) Section-II: Health Insurance (5 chapters) Section-III: General Insurance (6 chapters) as below I. Section- I : COMMON CHAPTERS (5 chapters) a. Chapter - 1: Introduction to Insurance kzbin.info/www/bejne/mpypgneMfZaCY8k b. Chapter - 2 Customer Service Chapter - 3: Grievance Redressal Mechanism kzbin.info/www/bejne/b3apfmV8ZdJ1bpI c. Chapter - 4: Regulatory aspects of Insurance Agents Chapter - 5: Legal Principle of an Insurance Contract kzbin.info/www/bejne/ppjZlK16nph9fcU II. Section - II: HEALTH INSURANCE (5 chapters) d. Chapter - 6: Introduction to Health Insurance Chapter - 7: Insurance Documentation Chapter-8: Health Insurance Products Chapter-9: Health Insurance Underwriting Chapter-10: Health Insurance Claims kzbin.info/www/bejne/Y2XHiGBqgcath7c III. Section - III: GENERAL INSURANCE e. Chapter - 11: Principles of Insurance Chapter - 12: Documentation Chapter - 13: Theory and Practice of Premium Rating : Chapters 11, 12, 13: kzbin.info/www/bejne/fp2Ze2SwaaiLZ8k f. Chapter - 14: Personal and Retail Insurance Chapter - 15: Commercial Insurance Chapter - 16: Claims Procedure : Chapters: 14, 15, 16: kzbin.info/www/bejne/fmTdeaifp76Bd7s ______ C. HEALTH INSURANCE (STAND ALONE) Agent Exam IC 38 IRDAI New Syllabus: Total 10 chapters divided into TWO Sections Section-I: Common chapters (5 chapters) Section-II: Health Insurance (5 chapters) as below I. Section- I : COMMON CHAPTERS (5 chapters) a. Chapter - 1: Introduction to Insurance kzbin.info/www/bejne/mpypgneMfZaCY8k b. Chapter - 2 Customer Service Chapter - 3: Grievance Redressal Mechanism kzbin.info/www/bejne/b3apfmV8ZdJ1bpI c. Chapter - 4: Regulatory aspects of Insurance Agents Chapter - 5: Legal Principle of an Insurance Contract kzbin.info/www/bejne/ppjZlK16nph9fcU II. Section - II: HEALTH INSURANCE (5 chapters) d. Chapter - 6: Introduction to Health Insurance Chapter - 7: Insurance Documentation Chapter-8: Health Insurance Products Chapter-9: Health Insurance Underwriting Chapter-10: Health Insurance Claims kzbin.info/www/bejne/Y2XHiGBqgcath7c 🙏 Please 👉SUBSCRIBE FREE 👍 & 🔔
@VenusAcademy Ай бұрын
Cannizzaro Reaction: _Overview_ The Cannizzaro reaction is a chemical reaction that involves the base-catalyzed disproportionation of an aldehyde to form an alcohol and a carboxylic acid. This reaction is a key process in organic synthesis. _General Reaction_ 2RCHO → RCH₂OH + RCOOH _Mechanism_ 1. Deprotonation of the aldehyde by base. 2. Formation of a hydride ion. 3. Nucleophilic attack by hydride on the aldehyde group. 4. Formation of an alkoxide ion. 5. Protonation of the alkoxide to form the alcohol. 6. Oxidation of the other aldehyde group to form the carboxylic acid. _Conditions_ 1. Base: Sodium hydroxide (NaOH) or potassium hydroxide (KOH). 2. Solvent: Water or ethanol. 3. Temperature: 50°C to 100°C. _Examples_ 1. Formaldehyde → Methanol + Formic acid 2. Benzaldehyde → Benzyl alcohol + Benzoic acid 3. Acetaldehyde → Ethanol + Acetic acid _Advantages_ 1. High yields. 2. Simple reaction conditions. 3. Useful for synthesizing alcohols and carboxylic acids. _Limitations_ 1. Limited scope for other aldehydes. 2. Requires strong base. 3. Can be slow. _Variations_ 1. Modified Cannizzaro reaction using phase-transfer catalysis. 2. Asymmetric Cannizzaro reaction using chiral catalysts. 3. Cannizzaro-type reactions with other carbonyl compounds. _Related Reactions_ 1. Benzoin condensation. 2. Aldol reaction. 3. Perkin reaction. _Applications_ 1. Organic synthesis. 2. Pharmaceutical chemistry. 3. Materials science. ❤😂🎉😢😮
@neharao523 Ай бұрын
Thank you sir i have passed the exam
@VenusAcademy Ай бұрын
@@neharao523 Congratulations Rao ji, wish you all the Best 🙏
@VenusAcademy Ай бұрын
Clemmensen Reduction: _Overview_ The Clemmensen reduction is a chemical reaction that reduces aldehydes or ketones to their corresponding hydrocarbons. This reaction is particularly useful for removing carbonyl groups (-C=O) from molecules. _General Reaction_ R-C(=O)-R' + 4Zn + 4HCl → R-CH₂-R' + 4ZnCl + 4H₂O _Mechanism_ 1. Formation of a zinc-carbonyl complex. 2. Reduction of the carbonyl group to a methylene group (-CH₂-). 3. Protonation of the intermediate. _Conditions_ 1. Solvent: Hydrochloric acid (HCl) or a mixture of HCl and ether. 2. Temperature: 0°C to 50°C. 3. Reducing agent: Zinc (Zn) metal. _Examples_ 1. Benzophenone → Diphenylmethane 2. Acetophenone → Ethylbenzene 3. Cyclohexanone → Cyclohexane _Advantages_ 1. High yields. 2. Mild conditions. 3. Useful for removing carbonyl groups. _Limitations_ 1. Limited scope for certain functional groups. 2. Requires zinc metal. 3. Can be slow. _Variations_ 1. Wolff-Kishner reduction (hydrazine and base). 2. Huang-Minlon modification (using diethylene glycol). 3. Catalytic hydrogenation. _Related Reactions_ 1. Wolff-Kishner reduction. 2. Huang-Minlon reduction. 3. Hydrogenation reactions.
@VenusAcademy Ай бұрын
IIT JEE Advanced 3 years Previous Question Papers with solutions (Maths, Physics, Chemistry) ▶2024 IIT JEE Advanced paper 1 answer key official by NTA: kzbin.info/www/bejne/iGe3l56hd6lqZ6s ▶2024 IIT JEE Advanced paper 2 answer key official by NTA: kzbin.info/www/bejne/poexiYh5hL5or8k ▶2023 IIT JEE Advanced paper 1 answer key official by NTA: kzbin.info/www/bejne/Y3iymomXap2Bo7csi=2QNMpEOzgZpM-eVK ▶2023 IIT JEE Advanced paper 2 answer key official by NTA: kzbin.info/www/bejne/nKenkoqhZa2MY8ksi=seiJtcKIgc2b_9Rr ▶2022 IIT JEE Advanced Paper 1 answer key official by NTA: kzbin.info/www/bejne/gF7UfGxjaJVlpq8si=5UkzFs2IzyUOzGLX ▶2022 IIT JEE advanced paper 2 answer key official by NTA: kzbin.info/www/bejne/kJmQqKOqjbx2b68si=rDSQ1DAu5g47Roug 🙏Please Subscribe @VenusAcademy 🙏
@VenusAcademy Ай бұрын
1💁🏻𝗗𝗼𝘄𝗻𝗹𝗼𝗮𝗱 𝟭𝟬 𝐩𝐫𝐞𝐯𝐢𝐨𝐮𝐬 𝐲𝐞𝐚𝐫 𝐐𝐮𝐞𝐬𝐭𝐢𝐨𝐧 𝐏𝐚𝐩𝐞𝐫 𝐰𝐢𝐭𝐡 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧 | NEET 👉 sites.google.com/site/venuschemistryacademy/exams/csir-ugc-net 2019 NEET: kzbin.info/www/bejne/eITGeJppqNOEgc0si=P2dASJZeizGsR2Aw 2020 NEET: kzbin.infopO19nGZYdMw?si=1m3rRk59B58sLM_n 2020 NEET: kzbin.infon9oDMHCZPgo?si=vOFSvfv1g1CnbayV 2021 NEET: kzbin.info/www/bejne/qpDcmqaFfZqloqMsi=vTQv6ncv71QVDfTh 2022 NEET: kzbin.info/www/bejne/pIbEpYJ6qNiUoK8si=qmuR4QZjiRuk2dTb 2023 NEET: kzbin.info/www/bejne/fWW5Y619ZbyIfrssi=wE6M25K_sEAjwkHD 2024 NEET: kzbin.info/www/bejne/iGS7k4Smbs-Nbtk @VenusAcademy 🙏Please Subscribe, Like & Share Venus Academy
@VenusAcademy Ай бұрын
GATE Previous 5 Years Chemistry (CY) Question Papers with Solutions - Google App (Free): sites.google.com/site/venuschemistryacademy/exams/gate-barc ☑ 2024 GATE - Chemistry (CY) : kzbin.info/www/bejne/h5CyqJ2Bd5WAgbs PDF Download with solutions: drive.google.com/file/d/1knDgK71lh2_cz0lpityz2kSIO_WkjV4F/view ☑ 2023 GATE - Chemistry (CY) : kzbin.info/www/bejne/a5ybg2Ojbrlpnrc PDF Download with solutions: drive.google.com/file/d/1_XwOPgjUqWZlWtZeT-GTcMq4GEjG7i15/view?usp=sharing ☑ 2022 GATE - Chemistry (CY) : kzbin.info/www/bejne/j4utZKOphNCEgbs PDF Download with solutions: drive.google.com/file/d/1pyJ9JEDCnn1SJxJDR5GnPoC-FmJwBVha/view?usp=sharing ☑ 2021 GATE - Chemistry (CY) : kzbin.info/www/bejne/jKepooaCpbJ8n6ssi=Qz0EP6UnKVP_VpCa PDF Download with solutions: drive.google.com/file/d/1RkfG5kANp1G1xO9k1ugPjjGN3asJXHbb/view?usp=sharing ☑ 2020 GATE - Chemistry (CY) : kzbin.infomMG9RctnmAc?si=NqXu5WfBOhqcei5D PDF Download: gate.iitd.ac.in/gate2020/CYPaper.php solutions: gate.iitd.ac.in/gate2020/CYKey.php @VenusAcademy 🙏Please Subscribe, Like & Share Venus Academy #gate #preparation #tips Preparing for the GATE exam in Chemistry can be challenging, but with the right strategies, you can maximize your effectiveness. Here are some tips to help you prepare: 1. Understand the Syllabus Familiarize yourself with the GATE Chemistry syllabus. Focus on key areas such as Physical Chemistry, Inorganic Chemistry, Organic Chemistry, and Analytical Chemistry. 2. Create a Study Plan Develop a structured study schedule that allocates time for each subject. Include breaks and review periods to reinforce learning. 3. Use Standard Textbooks Rely on standard textbooks for in-depth understanding. Books like: Physical Chemistry by Peter Atkins Organic Chemistry by Morrison and Boyd Inorganic Chemistry by J.D. Lee Analytical Chemistry by Harris 4. Focus on Concepts Build a strong conceptual foundation rather than just memorizing facts. Understanding the principles will help you tackle application-based questions. 5. Practice Numerical Problems Physical Chemistry often involves numerical problems. Practice as many problems as possible, and familiarize yourself with the types of calculations required. 6. Solve Previous Year Papers Work on previous GATE exam papers to understand the pattern, difficulty level, and frequently asked topics. Time yourself to improve your speed. 7. Take Mock Tests Regularly take mock tests to assess your preparation level. This will also help you manage your time effectively during the actual exam. 8. Revise Regularly Schedule regular revision sessions to revisit topics you’ve studied. This helps reinforce your memory and understanding. 9. Join Study Groups Consider joining study groups or online forums. Discussing topics with peers can provide new insights and help clarify doubts. 10. Stay Updated Keep an eye on any updates regarding the GATE exam pattern or syllabus changes. 11. Focus on Weak Areas Identify your weak subjects or topics and dedicate extra time to improve in those areas. 12. Stay Healthy Don’t neglect your health. Ensure you get enough sleep, eat well, and take breaks to avoid burnout. 13. Seek Help When Needed If you’re struggling with specific topics, don’t hesitate to seek help from teachers or online resources. 14. Stay Positive and Motivated Keep a positive mindset and stay motivated. Remind yourself of your goals and celebrate small achievements along the way. By following these tips and maintaining a disciplined approach, you'll enhance your preparation and increase your chances of success in the GATE Chemistry exam. Good luck!
@VenusAcademy Ай бұрын
💁🏻𝗗𝗼𝘄𝗻𝗹𝗼𝗮𝗱 𝟭𝟬 𝐩𝐫𝐞𝐯𝐢𝐨𝐮𝐬 𝐲𝐞𝐚𝐫 𝐐𝐮𝐞𝐬𝐭𝐢𝐨𝐧 𝐏𝐚𝐩𝐞𝐫 𝐰𝐢𝐭𝐡 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧 | 𝗖𝗦𝗜𝗥-𝗡𝗘𝗧 | 𝗜𝗜𝗧 𝗝𝗔𝗠 | 𝗚𝗔𝗧𝗘👉 sites.google.com/site/venuschemistryacademy/exams/csir-ugc-net 👉 CSIR UGC NET - 2024 June 29th - Chemistry - kzbin.info/www/bejne/qXvTq5Jtq52Jm68 PDF Download with solutions: drive.google.com/file/d/1m2nX8xAQQojZQIs897eHt1Ql9TzVuGm7/view?usp=sharing 👉 CSIR UGC NET - 2023 December 27th - Chemistry - kzbin.info/www/bejne/rX-am3pso9irf7M PDF Download with solutions: drive.google.com/file/d/18vFz-T8gSCYjEjOjH2tVrcqp8VNYTLqx/view?usp=sharing 👉 CSIR UGC NET - 2023 June 7th - Chemistry - kzbin.info/www/bejne/i5vdfWiOaJeYqKs PDF Download with solutions: drive.google.com/file/d/1LRok2-oHilvzkV0fg2KVaMCl1haURK5t/view 👉 CSIR UGC NET - 2022 Feb 16th - Chemistry kzbin.info/www/bejne/ipOqmaiggtuKp9U PDF Download with solutions: drive.google.com/file/d/1_d68vw2mGVHwRAPQfecKXxKsBOB8DBCt/view 👉 CSIR UGC NET - 2019 December 15th - Chemistry docs.google.com/forms/d/e/1FAIpQLSdFea-H7pS9bO129_5CUeD_wd0kNg5m09otvYOSAW1d5dsXVw/viewform PDF Download with solutions: drive.google.com/file/d/1WRwk2C8xdu1CkjS2dADiIOBWK2xFfurt/view # venusacademy
@VenusAcademy Ай бұрын
💁🏻𝗗𝗼𝘄𝗻𝗹𝗼𝗮𝗱 𝟭𝟬 𝐩𝐫𝐞𝐯𝐢𝐨𝐮𝐬 𝐲𝐞𝐚𝐫 𝐐𝐮𝐞𝐬𝐭𝐢𝐨𝐧 𝐏𝐚𝐩𝐞𝐫 𝐰𝐢𝐭𝐡 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧 | 𝗖𝗦𝗜𝗥-𝗡𝗘𝗧 | 𝗜𝗜𝗧 𝗝𝗔𝗠 | 𝗚𝗔𝗧𝗘👉 sites.google.com/site/venuschemistryacademy/exams/csir-ugc-net 👉 IIT JAM - 2022 Chemistry video solutions: kzbin.info/www/bejne/hWbPhaxve5d6nrM 👉 IIT JAM - 2022 Chemistry PDF with solutions: drive.google.com/file/d/1E20zu3ZJTQgy-RgYqo_mHBGbJZmI9QDI/view?usp=sharing 👉 IIT JAM - 2021 Chemistry - kzbin.info/www/bejne/mp3UnJmwrslgoqs PDF Download with solutions: drive.google.com/file/d/1_loPCMISBkOhThsn4gVOpHNkm5LyHhdx/view?usp=sharingkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.pngkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.png 👉 IIT JAM - 2020 Chemistry - kzbin.info/www/bejne/p4bYq4F-lJucn9U PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfDrPk9QsBorTT-1Vgn16IWUnHkQhdf4LOcvbK-cWmuXrp_kw/viewform 👉 IIT JAM - 2019 Chemistry - kzbin.info/www/bejne/fqKQhmONic-lqdE PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfqV4b9Yp67rq0Ce9I6uSzNLlGMXZ1ByjGfatMsS-f5IjILTw/viewform?usp=send_form 👉 IIT JAM - 2018 Chemistry - kzbin.info/www/bejne/imOWpZ2QhJd7mpo PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLScRnQVr1GP8W0xs3zH4yFkRwI3S0n9QO8fliAxKDtCU6vyU6w/viewform
@JOYMATIDEKAVlogs Ай бұрын
Joy Surya joy❤❤❤❤❤
@VenusAcademy Ай бұрын
Thank you madam for your comments.. wish you all the best
@JOYMATIDEKAVlogs Ай бұрын
Joy duryajoy ❤❤❤❤❤
@VenusAcademy Ай бұрын
Jai Surya Deva.... Surya Namaskar.. wish you all the best.
@TVAruna-gg7vn Ай бұрын
Sir thank you so much I passed today with 35 marks. I only watch ur all videos and scored very happy to share. Guys go study here really worth studying..
@VenusAcademy Ай бұрын
But-2-ene Reaction with Chlorofluorocarbene: Overview Chlorofluorocarbene (:CFCl) is a highly reactive intermediate that reacts with but-2-ene through a cycloaddition mechanism. General Reaction CH₃CH=CHCH₃ + :CFCl → CH₃C(Cl)FCH(CH₃) Mechanism 1. Electrophilic attack by :CFCl on the alkene. 2. Formation of a three-membered ring (cyclopropane) intermediate. 3. Ring-opening to form the addition product. Conditions 1. Catalyst: Phase transfer catalysts (e.g., tetrabutylammonium bromide). 2. Solvent: Polar solvents like dichloromethane or acetonitrile. 3. Temperature: -20°C to 50°C. 4. Pressure: Atmospheric. Examples 1. But-2-ene + :CFCl → 1-Chloro-2-fluoro-2-methylcyclopropane 2. But-2-ene + :CFCl → 1-Chloro-2-fluoro-3-methylcyclopropane Product Distribution 1. Stereospecific addition ( syn- or anti-). 2. Regioselectivity. Advantages 1. High yields. 2. Stereoselectivity. 3. Useful for synthesizing fluorinated compounds. Limitations 1. Highly reactive :CFCl intermediate. 2. Requires careful handling. 3. Limited scope for complex alkenes. Variations 1. Generation of :CFCl from chlorofluoromethane (CH₃CFCl). 2. Asymmetric synthesis using chiral catalysts. 3. Microwave-assisted reaction. Related Reactions 1. Cyclopropanation reactions. 2. Electrophilic addition of halogens. 3. Dichlorocarbene (:CCl₂) addition.
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Oxidation of Alkyl Arenes with KMnO4 (Potassium Permanganate): *Overview* KMnO4 is a strong oxidizing agent that cleaves alkyl arenes, converting them into carboxylic acids, aldehydes, or ketones. *General Reaction* R-Ph + KMnO4 → R-COOH, R-CHO, or R-CO-R' *Mechanism* 1. Electrophilic attack by MnO4- on the alkyl arene. 2. Formation of a radical intermediate. 3. Oxidative cleavage of the alkyl group. 4. Formation of carboxylic acid, aldehyde, or ketone. *Conditions* 1. Solvent: Water, acetone, or acetic acid. 2. Temperature: 0°C to 100°C. 3. Concentration: 1-5 equivalents of KMnO4. 4. Time: 30 minutes to 24 hours. *Examples* 1. Toluene → Benzoic acid 2. Ethylbenzene → Phenylacetic acid 3. Cumene → Acetophenone *Product Distribution* 1. Primary alkyl arenes → Carboxylic acids. 2. Secondary alkyl arenes → Ketones. 3. Tertiary alkyl arenes → No reaction. *Advantages* 1. High yields. 2. Mild conditions. 3. Useful for synthesizing carboxylic acids and ketones. *Limitations* 1. Over-oxidation can occur. 2. Sensitive to acidic conditions. 3. Limited scope for complex alkyl arenes. *Variations* 1. Catalytic KMnO4 oxidation. 2. Oxidation with KMnO4 in ionic liquids. 3. Microwave-assisted KMnO4 oxidation. *Related Reactions* 1. Chromium oxide (CrO3) oxidation. 2. Ruthenium tetroxide (RuO4) oxidation. 3. Ozonolysis. 🎉
@VenusAcademy Ай бұрын
Diels-Alder Reaction Stereochemistry Mechanism: *Overview* The Diels-Alder reaction is a [4+2] cycloaddition that forms a cyclic compound with high regio- and stereoselectivity. *Stereochemistry* 1. *Endo Rule*: The dienophile approaches the diene from the side that minimizes steric interactions, resulting in an endo product. 2. *Exo Rule*: The dienophile approaches the diene from the side that maximizes steric interactions, resulting in an exo product. 3. *Alder's Rule*: The product with the most stable configuration (endo or exo) is formed. *Mechanistic Steps* 1. *Approach*: The dienophile approaches the diene, forming a transition state. 2. *Cycloaddition*: The dienophile and diene form two new σ-bonds, creating a cyclic compound. 3. *Product Formation*: The product is formed with a specific stereochemistry. *Stereochemical Outcomes* 1. *cis-Addition*: The dienophile adds cis to the diene, forming a cis-product. 2. *trans-Addition*: The dienophile adds trans to the diene, forming a trans-product. 3. *Retentive Addition*: The configuration of the dienophile is retained in the product. *Factors Influencing Stereochemistry* 1. *Steric Effects*: Bulky substituents on the diene or dienophile influence approach and product stereochemistry. 2. *Electronic Effects*: Electron-withdrawing or electron-donating substituents influence reactivity and stereochemistry. 3. *Temperature and Pressure*: Conditions can influence product distribution. *Examples* 1. Cyclopentadiene + Acrylonitrile → 3-Cyanonorbornene (endo product) 2. Butadiene + Ethyl Acrylate → 3-Carbethoxy-4-cyclohexene (exo product) *Related Reactions* 1. Hetero-Diels-Alder reaction 2. Inverse Electron Demand Diels-Alder reaction 3. Catalytic Diels-Alder reaction 🎉😢😮
@VenusAcademy Ай бұрын
Stereospecific Reduction of Ketones using NaBH4: *Overview* NaBH4 (Sodium Borohydride) is a mild reducing agent commonly used for the stereospecific reduction of ketones to form secondary alcohols. *General Reaction* R1R2C=O + NaBH4 → R1R2CH-OH *Mechanism* 1. Nucleophilic attack by BH4- on the carbonyl carbon. 2. Formation of a tetrahedral intermediate. 3. Hydride transfer to the carbonyl carbon. 4. Protonation of the alkoxide intermediate. *Stereospecificity* NaBH4 reduction of ketones can exhibit stereospecificity due to: 1. Felkin-Anh model: Predicts the major diastereomer formed. 2. Cram's rule: Influences the stereoselectivity. *Factors Influencing Stereospecificity* 1. Ketone structure: Substituent size and orientation. 2. Reducing agent concentration. 3. Temperature. 4. Solvent. *Conditions* 1. Solvent: Ethanol, methanol, or THF. 2. Temperature: 0°C to 25°C. 3. Concentration: 1-5 equivalents of NaBH4. 4. Time: 30 minutes to 2 hours. *Examples* 1. Reduction of 2-butanone: Forms (S)-2-butanol. 2. Reduction of cyclohexanone: Forms trans-1,2-cyclohexanediol. *Advantages* 1. Mild conditions. 2. High yields. 3. Stereospecificity. *Limitations* 1. Limited scope for large-scale reductions. 2. Sensitive to acidic conditions. *Variations* 1. Asymmetric reduction using chiral auxiliaries. 2. Catalytic NaBH4 reduction. *Related Reactions* 1. LiAlH4 reduction. 2. DIBAL-H reduction. 3. Hydrogenation using H2 and catalysts. 🎉🎉😢🎉😅
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Carbon-Carbon Double Bond Formation Reactions: *1. Wittig Reaction* - RCH=O + Ph3P=CH2 → RCH=CH2 - Conditions: THF, reflux - Mechanism: Phosphorus ylide formation, nucleophilic attack *2. Horner-Wadsworth-Emmons Reaction* - RCH=O + (EtO)2P(O)CH2COOEt → RCH=CHCOOEt - Conditions: THF, NaH, reflux - Mechanism: Phosphonate ester formation, nucleophilic attack *3. Julia-Kocienski Olefination* - RCH=O + (PhSO2)2CHLi → RCH=CH2 - Conditions: THF, -78°C - Mechanism: Sulfone formation, nucleophilic attack *4. Takai Olefination* - RCH=O + CHI3 + Zn(Cu) → RCH=CH2 - Conditions: THF, reflux - Mechanism: Zinc-carbene formation, nucleophilic attack *5. McMurry Reaction* - 2RCHO → RCH=CHR - Conditions: TiCl3, Zn(Cu), reflux - Mechanism: Pinacol coupling, dehydration *6. Dehydration of Alcohols* - RCH(OH)CH2R → RCH=CHR - Conditions: Acid catalyst (e.g., H2SO4), heat - Mechanism: Protonation, elimination *7. Elimination Reactions (E1, E2)* - RCH2CH2X → RCH=CH2 - Conditions: Base (e.g., NaOH), heat - Mechanism: Protonation, elimination *8. Cross-Metathesis (CM)* - RCH=CH2 + R'CH=CH2 → RCH=CHR' - Conditions: Catalyst (e.g., Grubbs), solvent - Mechanism: Ruthenium-carbene formation, metathesis *9. Heck Reaction* - RCH=CH2 + ArX → RCH=CHAr - Conditions: Pd catalyst, solvent, base - Mechanism: Palladium-olefin complex formation, insertion *10. Suzuki Coupling* - RCH=CH2 + ArB(OH)2 → RCH=CHAr - Conditions: Pd catalyst, solvent, base - Mechanism: Palladium-olefin complex formation, cross-coupling 🎉
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Bromination of Pyrrole and Pyridine using Bromine in Ethanol: *Pyrrole Bromination* _Reaction:_ Pyrrole + Br2 → 2,3,4-Tribromopyrrole (major) + 2,3-Dibromopyrrole (minor) _Conditions:_ - Solvent: Ethanol - Temperature: 0°C to 5°C - Reaction time: 30 minutes to 1 hour - Bromine equivalent: 1-3 *Pyridine Bromination* _Reaction:_ Pyridine + Br2 → 3-Bromopyridine (major) + 2-Bromopyridine (minor) _Conditions:_ - Solvent: Ethanol - Temperature: 0°C to 50°C - Reaction time: 1-2 hours - Bromine equivalent: 1-2 *Mechanism:* 1. Electrophilic addition of bromine to the heterocyclic ring. 2. Formation of a σ-complex. 3. Loss of HBr to form the brominated product. *Factors Influencing Bromination:* 1. Solvent: Ethanol facilitates the reaction. 2. Temperature: Lower temperatures favor pyrrole bromination. 3. Bromine equivalent: Excess bromine can lead to polybromination. 4. Presence of catalysts (e.g., FeCl3) can enhance reactivity. *Importance:* 1. Synthesis of brominated heterocycles for pharmaceuticals. 2. Precursors to agrochemicals and materials. 3. Useful in the formation of complex molecules. *Precautions:* 1. Handle bromine with caution due to toxicity and reactivity. 2. Use protective equipment and ventilation. 3. Monitor reaction temperature and time. *Related Reactions:* 1. Chlorination of pyrrole and pyridine. 2. Iodination of pyrrole and pyridine. 3. Nitration of pyrrole and pyridine. 🎉
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Claisen Condensation Reaction of Nicotinaldehyde: *Reaction Overview* Nicotinaldehyde undergoes Claisen condensation with esters or carbonyl compounds to form substituted nicotinic acids or β-keto esters. *General Reaction* Nicotinaldehyde + RCOOR' → Nicotinic acid derivatives *Mechanism* 1. Deprotonation of nicotinaldehyde by a strong base (e.g., NaOEt). 2. Nucleophilic attack by the deprotonated aldehyde on the ester. 3. Formation of a tetrahedral intermediate. 4. Elimination of the leaving group (alkoxide). 5. Formation of the β-keto ester. *Conditions* 1. Strong base (e.g., NaOEt, KOtBu). 2. Polar aprotic solvent (e.g., THF, DMF). 3. Temperature: 0°C to 100°C. 4. Pressure: Atmospheric or elevated. *Examples* 1. Nicotinaldehyde + diethyl oxalate → Diethyl 6-cyanonicotinate. 2. Nicotinaldehyde + ethyl acetate → Ethyl 6-methyl-3-oxonicotinate. 3. Nicotinaldehyde + methyl 3-oxobutanoate → Methyl 6-(1-hydroxybut-3-en-2-yl)nicotinate. *Importance* 1. Synthesis of nicotinic acid derivatives with potential biological activity. 2. Precursors to pharmaceuticals and agrochemicals. 3. Useful in the formation of heterocyclic compounds. *Variations* 1. Intramolecular Claisen condensation. 2. Asymmetric Claisen condensation using chiral bases. 3. Solid-phase Claisen condensation. *Related Reactions* 1. Perkin reaction. 2. Knoevenagel condensation. 3. Wittig reaction. *Troubleshooting* 1. Incomplete reaction: Check reaction conditions, base, and solvent. 2. Side reactions: Monitor reaction progress, adjust conditions. 3. Low yield: Optimize reaction conditions, purify product.
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NMR Spectroscopy of Para-Methyl Benzyl Chloride: *1H NMR Spectrum:* - Chemical Shifts (δ, ppm): - 2.35 (s, 3H, -CH3) - 4.55 (s, 2H, -CH2Cl) - 7.25-7.45 (m, 4H, aromatic) - Coupling Constants (J, Hz): - J = 8.0 Hz (ortho coupling) *13C NMR Spectrum:* - Chemical Shifts (δ, ppm): - 21.5 (-CH3) - 44.5 (-CH2Cl) - 126.5, 129.2, 133.5, 138.5 (aromatic carbons) *Assignment:* - -CH3 (methyl group): 2.35 ppm - -CH2Cl (benzyl chloride): 4.55 ppm - C1 (ipso carbon): 138.5 ppm - C2/C6 (ortho carbons): 129.2 ppm - C3/C5 (meta carbons): 126.5 ppm - C4 (para carbon): 133.5 ppm *Solvent:* - CDCl3 (chloroform-d) *Instrument Parameters:* - 1H NMR: 400 MHz, 32k data points, 64 scans - 13C NMR: 100 MHz, 64k data points, 1024 scans *Interpretation:* - The 1H NMR spectrum shows three distinct signals: a singlet for the methyl group, a singlet for the benzyl chloride, and a multiplet for the aromatic protons. - The 13C NMR spectrum shows five distinct signals for the aromatic carbons and two signals for the methyl and benzyl chloride groups. - The chemical shifts and coupling constants are consistent with the structure of para-methyl benzyl chloride. *Related Spectroscopic Techniques:* - IR spectroscopy: to confirm the presence of the chloro and methyl groups. - MS spectroscopy: to determine the molecular weight and fragmentation pattern. - 2D NMR spectroscopy (e.g., COSY, HSQC): to confirm the assignment of signals. 🎉
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Michael Addition of HCN: _Reaction Overview:_ The Michael addition of HCN is a nucleophilic addition reaction where hydrogen cyanide (HCN) adds to an α,β-unsaturated carbonyl compound, resulting in the formation of a new carbon-carbon bond. _General Reaction:_ RCH=CH-C=O + HCN → RCH(CN)-CH2-C=O _Mechanism:_ 1. Nucleophilic attack by CN- (cyanide ion) on the β-carbon of the α,β-unsaturated carbonyl compound. 2. Formation of an enolate intermediate. 3. Protonation of the enolate by H+ (from HCN). _Conditions:_ 1. Base catalysis (e.g., NaOH, KOH) 2. Temperature: 0°C to 50°C 3. Solvent: Polar aprotic solvents (e.g., DMSO, DMF) _Examples:_ 1. Acrylaldehyde + HCN → 3-Hydroxy-2-methylpropanenitrile 2. Crotonaldehyde + HCN → 3-Hydroxy-2-methylbutanenitrile 3. Benzylideneacetone + HCN → 3-Hydroxy-2-phenyl-4-pentenenitrile _Importance:_ 1. Synthetic route to α-cyano ketones. 2. Precursor to pharmaceuticals and agrochemicals. 3. Useful in the synthesis of complex molecules. _Variations:_ 1. Stoichiometric addition of HCN. 2. Catalytic addition using Lewis acids (e.g., AlCl3). 3. Asymmetric Michael addition using chiral catalysts. _Related Reactions:_ 1. Michael addition of other nucleophiles (e.g., amines, alcohols). 2. Conjugate addition of organometallic reagents. 3. Cyanation reactions using other cyanide sources. 🎉
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The Joint Admission Test for Masters (JAM) has set the benchmark for undergraduate science education in the country for the past two decades. This prestigious exam paves the way for students to gain admission to top-tier postgraduate programs, solidifying science as a stellar career choice nationwide. Our programs offer world-class education in various disciplines, designed to cultivate academic excellence and a fulfilling professional life. What does JAM offer? JAM is not just an exam-it's a gateway to premier institutes offering high-quality postgraduate education. The interdisciplinary nature of the curriculum empowers students to translate scientific knowledge into real-world applications. These opportunities are open to all eligible students, regardless of nationality, with English as the medium of instruction. With a JAM score, you can pursue a range of advanced degrees, including: M.Sc. M.Sc. (Tech.) MS (Research) M.Sc. - M.Tech. Dual Degree Joint M.Sc. - Ph.D. M.Sc. - Ph.D. Dual Degree How Admissions Work Admissions through JAM 2025 are categorized into: Admitting Institutes: Coordinated by the JAM 2025 Organizing Institute. Result Sharing Institutes: Candidates must approach these institutes directly after qualifying. JAM 2025 Organizing Institute will coordinate the admission process of only the Admitting Institutes and the candidates can apply for Admission after qualifying the JAM 2025 examination. For admissions to Result Sharing Institutes qualifying candidates have to directly approach the respective Institute / admission body. Key Information for JAM 2025 Exam Date: February 2, 2025 (Sunday) Format: Computer-Based Test (CBT) across seven subjects: Biotechnology, Chemistry, Economics, Geology, Mathematical Statistics, Mathematics, and Physics. Locations: Conducted in approximately 100 cities across India. Eligibility: Open to all nationalities, with no age restriction. Candidates completing their qualifying degrees in 2025 are eligible. Admission Criteria All India Rank (AIR): Admission is based on AIR in each test paper, reservation policies (Govt. of India), and seat availability. Foreign Nationals: Must comply with the respective Admitting Institute's regulations. Requirements: The candidates who have either completed or will be appearing in the final examination of their qualifying degree in 2025 are eligible to appear in JAM 2025. By qualifying in JAM 2025, candidates can apply for admission subject to the conditions that all parts of their undergraduate programme shall be completed before the date of admission of the respective Admitting Institute, and proof of having passed the qualifying degree with required eligibility, as specified by the Admitting Institute should be submitted within the timeline provided by respective admitting institute. The list of academic programmes, number of seats, Eligibility Requirements (ERs) and Minimum Educational Qualifications (MEQs) of each of the programmes mentioned in the Information Brochure are subject to change, as per the policy of Admitting Institutes. In all matters concerning JAM 2025, the decision of the Organizing Institute, JAM 2025 will be final and binding on all the applicants #csir #gate #iit #jam #chemistry #physics #maths 💁🏻𝗗𝗼𝘄𝗻𝗹𝗼𝗮𝗱 𝟭𝟬 𝐩𝐫𝐞𝐯𝐢𝐨𝐮𝐬 𝐲𝐞𝐚𝐫 𝐐𝐮𝐞𝐬𝐭𝐢𝐨𝐧 𝐏𝐚𝐩𝐞𝐫 𝐰𝐢𝐭𝐡 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧 | 𝗖𝗦𝗜𝗥-𝗡𝗘𝗧 | 𝗜𝗜𝗧 𝗝𝗔𝗠 | 𝗚𝗔𝗧𝗘👉 sites.google.com/site/venuschemistryacademy/exams/csir-ugc-net 👉 IIT JAM - 2021 Chemistry - kzbin.info/www/bejne/mp3UnJmwrslgoqs PDF Download with solutions: drive.google.com/file/d/1_loPCMISBkOhThsn4gVOpHNkm5LyHhdx/view?usp=sharingkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.pngkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.png 👉 IIT JAM - 2020 Chemistry - kzbin.info/www/bejne/p4bYq4F-lJucn9U PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfDrPk9QsBorTT-1Vgn16IWUnHkQhdf4LOcvbK-cWmuXrp_kw/viewform 👉 IIT JAM - 2019 Chemistry - kzbin.info/www/bejne/fqKQhmONic-lqdE PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfqV4b9Yp67rq0Ce9I6uSzNLlGMXZ1ByjGfatMsS-f5IjILTw/viewform?usp=send_form 👉 IIT JAM - 2018 Chemistry - kzbin.info/www/bejne/imOWpZ2QhJd7mpo PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLScRnQVr1GP8W0xs3zH4yFkRwI3S0n9QO8fliAxKDtCU6vyU6w/viewform
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💁🏻𝗗𝗼𝘄𝗻𝗹𝗼𝗮𝗱 𝟭𝟬 𝐩𝐫𝐞𝐯𝐢𝐨𝐮𝐬 𝐲𝐞𝐚𝐫 𝐐𝐮𝐞𝐬𝐭𝐢𝐨𝐧 𝐏𝐚𝐩𝐞𝐫 𝐰𝐢𝐭𝐡 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧 | 𝗖𝗦𝗜𝗥-𝗡𝗘𝗧 | 𝗜𝗜𝗧 𝗝𝗔𝗠 | 𝗚𝗔𝗧𝗘👉 sites.google.com/site/venuschemistryacademy/exams/csir-ugc-net 👉 IIT JAM - 2021 Chemistry - kzbin.info/www/bejne/mp3UnJmwrslgoqs PDF Download with solutions: drive.google.com/file/d/1_loPCMISBkOhThsn4gVOpHNkm5LyHhdx/view?usp=sharingkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.pngkzbin.infogaming/emoji/7ff574f2/emoji_u1f449.png 👉 IIT JAM - 2020 Chemistry - kzbin.info/www/bejne/p4bYq4F-lJucn9U PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfDrPk9QsBorTT-1Vgn16IWUnHkQhdf4LOcvbK-cWmuXrp_kw/viewform 👉 IIT JAM - 2019 Chemistry - kzbin.info/www/bejne/fqKQhmONic-lqdE PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLSfqV4b9Yp67rq0Ce9I6uSzNLlGMXZ1ByjGfatMsS-f5IjILTw/viewform?usp=send_form 👉 IIT JAM - 2018 Chemistry - kzbin.info/www/bejne/imOWpZ2QhJd7mpo PDF Download with solutions: docs.google.com/forms/d/e/1FAIpQLScRnQVr1GP8W0xs3zH4yFkRwI3S0n9QO8fliAxKDtCU6vyU6w/viewform
@raniraonivi6787 Ай бұрын
16th question answer.. B?
@VenusAcademy Ай бұрын
Thank you Rani ji, wish you all the best.
@raniraonivi6787 Ай бұрын
23rd question from another channel they said answer - Insurance company shareholders Question ( who among the following is not a stake holder in insurance claim process) Please explain
@VenusAcademy Ай бұрын
Given answer is correct only. wish you all the best.
@raniraonivi6787 Ай бұрын
@VenusAcademy thanks for your kind reply... 4 or 5 questions only came from all vedios.(not only yours) .. I atten 13/11/2024... (General insurance) we want to know more details to write exam... Got 27 marks 🙏 Anyway Very Thanks for your Hard work 🙏🙏🙏🙏🙏
@VenusAcademy Ай бұрын
@@raniraonivi6787 Congratulations... wish you all the best.🙏
@Zaraki007 2 ай бұрын
Very thankyou ❤
@VenusAcademy Ай бұрын
@@Zaraki007 Thank you ji, Wish you all the best 🙏
@Zaraki007 Ай бұрын
@VenusAcademy Thanks Bro I passed with 35 marks🥰
@VenusAcademy Ай бұрын
@@Zaraki007 Congratulation.... wish you All the best.
@VenusAcademy 2 ай бұрын
If you are born poor, it's not your fault. But if you die poor it's your mistake 🎉
@lankakalavathi9444 2 ай бұрын
Sir ic 38 exam English lo untada telugu lo untada
@VenusAcademy 2 ай бұрын
@@lankakalavathi9444 Dear Madam, this exam is conducted in all 11 languages like English, Hindi, Telugu, Bengali etc.. So, if you want you can write this exam in Telugu.efium also, all the Best 🙏
@VenusAcademy 2 ай бұрын
KYC (Know Your Customer) Norms for Insurance Policies: *Objective:* To prevent and detect insurance fraud, money laundering, and terrorist financing by verifying the identity of policyholders and beneficiaries. *Regulatory Framework:* 1. Insurance Regulatory and Development Authority of India (IRDAI) guidelines 2. Prevention of Money Laundering (PML) Act, 2002 3. Financial Action Task Force (FATF) recommendations *KYC Requirements:* *Individual Policyholders:* 1. Identity proof: - Passport - Driving license - Voter ID card - Aadhaar card 2. Address proof: - Utility bills (electricity, water, gas) - Bank statement - Passport 3. Date of birth proof: - Birth certificate - Passport - Driving license 4. PAN card (for policies with annual premium > ₹50,000) *Non-Individual Policyholders (e.g., Companies, Trusts):* 1. Certificate of incorporation 2. Memorandum and Articles of Association 3. PAN card 4. Identity proof of authorized signatories 5. Address proof of the organization *Beneficiary KYC:* 1. Identity proof 2. Address proof 3. Relationship proof (with policyholder) *Additional Requirements:* 1. Source of funds/funds declaration 2. Occupation and income proof (for high-value policies) 3. Politically Exposed Person (PEP) declaration *Verification Process:* 1. In-person verification 2. Document-based verification 3. Electronic verification (e.g., Aadhaar-based) *Ongoing Customer Due Diligence:* 1. Regular updates of policyholder information 2. Monitoring of suspicious transactions 3. Periodic review of beneficiary information *Consequences of Non-Compliance:* 1. Policy cancellation 2. Delayed claim settlements 3. Regulatory penalties 4. Reputation risk *Insurance Company Obligations:* 1. Establish robust KYC policies and procedures 2. Train employees on KYC/AML regulations 3. Conduct regular audits and reviews 4. Report suspicious transactions to Financial Intelligence Unit (FIU) *Customer Responsibilities:* 1. Provide accurate and complete information 2. Update information promptly 3. Cooperate during verification process 🎉
@VenusAcademy 2 ай бұрын
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@SphoortiS 2 ай бұрын
The Bhagavad Gita has 18 chapters, each with its own unique insights and teachings. Here's an overview of the chapters: Chapter 1: Arjuna's Dilemma - The setting of the Gita is established, and Arjuna's conflict begins. Chapter 2: Sankhya Yoga - The nature of the self and the path to liberation. Chapter 3: Karma Yoga - The path of action without attachment. Chapter 4: Jnana Yoga - The path of knowledge. Chapter 5: Karma-Sannyasa Yoga - Renunciation of action. Chapter 6: Dhyana Yoga - The path of meditation. Chapter 7: Jnana-Vijnana Yoga - Knowledge and realization. Chapter 8: Akshara-Para-Brahma Yoga - The imperishable absolute. Chapter 9: Rajavidya Rajaguhya Yoga - The royal science and royal secret. Chapter 10: Vibhuti Yoga - The divine manifestations. Chapter 11: Visvarupa-Darshana Yoga - The vision of the universal form. Chapter 12: Bhakti Yoga - The path of devotion. Chapter 13: Kshetra-Kshetrajna Vibhaga Yoga - The field and the knower. Chapter 14: Gunatraya Vibhaga Yoga - The three modes. Chapter 15: Purushottama Yoga - The supreme person. Chapter 16: Daivasura-Sampad-Vibhaga Yoga - Divine and demonic qualities. Chapter 17: Shraddhatraya Vibhaga Yoga - The threefold faith. Chapter 18: Moksha-Sannyasa Yoga - Liberation through renunciation.
@SphoortiS 2 ай бұрын
Bhagavad Gita, Chapter 1: Arjuna's Dilemma (Arjuna-Vishada Yoga) *Overview:* Chapter 1 sets the stage for the Gita, introducing the main characters, setting, and conflict. Arjuna, faced with the prospect of battling his kin, experiences emotional turmoil and moral dilemma. *Key Verses:* 1. Verse 1: "Dhritarashtra asks Sanjaya to describe the scene on the battlefield." 2. Verse 20: "Arjuna sees his kin and friends on the opposing side." 3. Verse 28: "Arjuna's emotional distress and moral confusion." 4. Verse 45: "Arjuna's despair and decision to abandon the fight." *Main Topics:* 1. *The Setting*: The battlefield of Kurukshetra, the opposing armies. 2. *Arjuna's Conflict*: Torn between duty (dharma) and compassion. 3. *Moral Dilemma*: Arjuna's concerns about harming his kin. 4. *Krishna's Introduction*: Krishna's presence as Arjuna's charioteer and guide. *Philosophical Insights:* 1. *Dharma*: The importance of fulfilling one's duty. 2. *Attachment*: Arjuna's attachment to his kin and friends. 3. *Conflict between Heart and Duty*: The struggle between emotions and responsibility. 4. *Seeking Guidance*: Arjuna turns to Krishna for wisdom. *Life Lessons:* 1. *Recognize moral conflicts*: Acknowledge inner turmoil. 2. *Seek guidance*: Turn to wise mentors or spiritual guides. 3. *Prioritize duty*: Fulfill responsibilities despite personal challenges. 4. *Cultivate detachment*: Balance emotions with rational thinking. *Reflection Questions:* 1. Have you faced similar moral dilemmas? How did you resolve them? 2. What are your priorities: duty, compassion, or personal interests? 3. How do you balance emotions and rational thinking? 4. Who are your guides or mentors in times of uncertainty? *Connection to Other Chapters:* Chapter 1 lays the foundation for the Gita's exploration of: 1. Karma Yoga (Chapter 3) 2. Bhakti Yoga (Chapter 12) 3. Dhyana Yoga (Chapter 6)
@SphoortiS 2 ай бұрын
Bhagavad Gita, Chapter 6: Dhyana Yoga (The Yoga of Meditation) *Overview:* Chapter 6 explores the path of meditation (Dhyana Yoga) as a means to attain self-realization and union with the Divine. Krishna guides Arjuna on the practices and principles necessary for effective meditation. *Key Verses:* 1. Verse 1: "One who performs prescribed duties without attachment to results is a yogi." 2. Verse 6: "The mind is the friend of the conditioned soul, and his enemy." 3. Verse 11: "Sit comfortably, with spine straight, and focus on the Self." 4. Verse 20: "When the mind, controlled by practice, becomes calm and tranquil..." 5. Verse 23: "The supreme bliss, beyond human understanding, is achieved." *Main Topics:* 1. *Characteristics of a Yogi*: Krishna outlines the qualities of a yogi, including detachment, self-control, and equanimity. 2. *Meditation Techniques*: Krishna provides practical instructions on meditation posture, breathing, and focus. 3. *Mind Control*: The importance of controlling the mind through practice (abhyasa) and detachment (vairagya). 4. *Self-Realization*: The ultimate goal of meditation is to realize one's true nature (Atman) and union with the Divine (Brahman). 5. *Obstacles and Solutions*: Krishna discusses common obstacles to meditation and offers solutions. *Philosophical Insights:* 1. *Duality of Mind*: The mind can be both friend and enemy. 2. *Importance of Self-Control*: Control over the senses and mind is essential. 3. *Non-Attachment*: Attachment to results hinders spiritual growth. 4. *Union with the Divine*: Meditation leads to union with the ultimate reality. *Life Lessons:* 1. *Cultivate detachment*: Perform actions without attachment to results. 2. *Practice mindfulness*: Focus on the present moment. 3. *Control your mind*: Develop self-awareness and self-regulation. 4. *Seek inner peace*: Meditation leads to supreme bliss. *Reflection Questions:* 1. What are the qualities of a yogi, and how can I cultivate them? 2. How can I control my mind and overcome obstacles in meditation? 3. What is the significance of self-realization, and how can I achieve it?
@SphoortiS 2 ай бұрын
The Bhagavad Gita has 18 chapters, each with its own unique insights and teachings. Here's an overview of the chapters: Chapter 1: Arjuna's Dilemma - The setting of the Gita is established, and Arjuna's conflict begins. Chapter 2: Sankhya Yoga - The nature of the self and the path to liberation. Chapter 3: Karma Yoga - The path of action without attachment. Chapter 4: Jnana Yoga - The path of knowledge. Chapter 5: Karma-Sannyasa Yoga - Renunciation of action. Chapter 6: Dhyana Yoga - The path of meditation. Chapter 7: Jnana-Vijnana Yoga - Knowledge and realization. Chapter 8: Akshara-Para-Brahma Yoga - The imperishable absolute. Chapter 9: Rajavidya Rajaguhya Yoga - The royal science and royal secret. Chapter 10: Vibhuti Yoga - The divine manifestations. Chapter 11: Visvarupa-Darshana Yoga - The vision of the universal form. Chapter 12: Bhakti Yoga - The path of devotion. Chapter 13: Kshetra-Kshetrajna Vibhaga Yoga - The field and the knower. Chapter 14: Gunatraya Vibhaga Yoga - The three modes. Chapter 15: Purushottama Yoga - The supreme person. Chapter 16: Daivasura-Sampad-Vibhaga Yoga - Divine and demonic qualities. Chapter 17: Shraddhatraya Vibhaga Yoga - The threefold faith. Chapter 18: Moksha-Sannyasa Yoga - Liberation through renunciation.