Reduction of Ketones and Aldehdyes Made Easy! - Organic Chemistry

[@canenjbellsouthnet]

THANK YOU FRANK!!!! I especially enjoy the explanations behind the reactions. AWESOME --- SIMPLY AMAZING FRANK

[@OrgoMadeEasy]

Thanks! :] Really appreciate the awesome feedback from you guys! Hope you did well on your exams.

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why at the end of semester i found this channel , if i would find it earlier my grade would be good, thanks man u are so great at explaining

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I subscribed as soon as I saw the intro! Looking forward to these videos. 😂😂😂

[@OrgoMadeEasy]

😂👍🏼 welcome to Orgo Made Easy!

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You guys are so awesome! I love the new intros, and the cool seque clip! Thanks for another great video. I don't know how you do it!!

[@OrgoMadeEasy]

Thanks Drew! Really appreciate the support from you. :] I'm currently working on the mechanism video+bloopers so keep an eye out. haha

[@lamaal-ahmadi6122]

Really I smile when watch your video you make the Organic Chemistry more easy Thanks ^^

[@OrgoMadeEasy]

Lama Al-Ahmadi Haha thanks Lama! That's awesome to hear. :] I'm glad my vid. could do that for you. Gluck studying!

[@yasmineabodief7156]

Thank you very much.you make this easier for me 😊😊

[@ShotClanTxter]

Is there like some sort of homework or practice problems i can do to help supplement learning? Im suppose to be a chem major but i dropped a nice C on o chem 1 :/ and i really want the A on o chem 2.

[@OrgoMadeEasy]

ShotClanTxter Sorry to hear, but I'm sure you can do it. I went from a B to an A and I've had students start off with a F in Orgo I and end with an A-. ;) Here are some problems, with solutions. You need to scroll down to the reduction portion of the article. :] www2.chemistry.msu.edu/faculty/reusch/virttxtjml/aldket1.htm

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You are so good, I love all of your videos! Thanks so much!

[@OrgoMadeEasy]

Beckkkahhhx3 Thanks for the feedback Becka! :] It's because of students like you give me all the motivation to keep going at it. :D

[@hardikminocha3149]

Hey! Can't we use DIBAL-H for this kind of reduction? It Also preserves the unsaturation in the Alkane, right?

[@OrgoMadeEasy]

Hey Hardik I'm not sure actually but the only time I've seen DIBAL-H is for reducing Esters to Aldehydes so it makes me think DIBAL-H wouldn't reduce the Aldehyde nor Alkene. Another unique reagent that's good to keep in mind is LiAl(OTBu)3-H which is extremely similar to DIBAL-H in that it can convert a Acyl Chloride into an Aldehyde.

[@thetearsofjungkook4985]

Im depending on these videos to get me into university...

[@MissSharon95]

Great video! Thank you

[@OrgoMadeEasy]

MissSharon95 Your welcome! I'm glad you liked it. :D

[@andrewmiller407]

I don't like your choice of example compounds. The products of the sodium borohydride reduction will tautomerize back to a ketone and aldehyde.

[@ashtyb8798]

can u please do video on the preparation of aldehydes and ketone from esters?

[@tejasbhukal9411]

can we reduce carboxylic acid to make ketone

[@OrgoMadeEasy]

Tejas Bhukal Hmm off the top of my mind I don’t think you can do it in one step. If you treat Carb Acid w SOCl2 and turn it into an Acid Chloride and then treat it with 1 Equiv of a Gilman Reagant ie (CH3-Cu-CH3) you can attack the carbonyl with a CH3 and kick off the Cl. And end up with a Ketone with CH3 as one of its R groups.

[@tejasbhukal9411]

@@OrgoMadeEasy thank you sir for your answer. i got it what you wanted to say of show . thanks again

[@tejasbhukal9411]

@@OrgoMadeEasy what's gilman reagant

[@mahnoor2768]

REDUCING AGENT DEFINITION MADE EASY !!

[@1234nicklim]

You're awesome. Keep going.

[@OrgoMadeEasy]

+Nikki Lim I'm going I'm going! lol In the meantime if you want other great resources for Orgo make sure you know about these guys/gals kzbin.info/www/bejne/Z4LOeKuHeK5km9U

[@thedrhinger7904]

You are the best!

[@OrgoMadeEasy]

Thanks Thed! Glad these vids are still coming in handy 😊!

[@OrgoMadeEasy]

Happy Studying! 💪🏼

[@hitenshah9]

which is the other reducing agent that reduces both alkene and the double bond in acids

[@hitenshah9]

sorry I meant to alkene and ketone /aldehyde I don't want to preserve the alkene and reduce both then which reducing agent should I use?

[@OrgoMadeEasy]

+hiten shah H2, Pt or H2, Ni both should do the trick :]

[@hitenshah9]

+Frank Wong Thanks :)

[@hardikminocha3149]

You can use Sn-HCl.

[@trinhtuan23]

tks so much. can i follow you ? your exm very easy

[@OrgoMadeEasy]

Of course you can Trinh. :] Thanks for watching! You can subscribe via KZbin to my channel and if you have a facebook just look up "Orgo Made Easy" and you should be able to find my facebook page.

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Frank you my angel... bless you x 24578887 millions times ... te amo

[@ashtyb8798]

awesome

[@mahedihasanmojumder7578]

Are you Korean ??

[@soujanyasou736]

so good