Good details and explanation was clear and concise. Only problem I face with Ochem in college is solving more complicated reactions and compounds. I think I should actually practice problems from the book more often.
@vedant80023 жыл бұрын
Are you alive?
@MrSmudger68713 жыл бұрын
@TheCarnagekidd6 - yes you can but thionyl chloride is preferable as the by products of the reaction (HCl and SO2) are both gaseous.
@Darkstar88Gaming12 жыл бұрын
good job!! explains alot! you da man, man!!!!
@vedantsinha7374 Жыл бұрын
thank you !
@MrTitchfield12 жыл бұрын
quite effectiive and explanation is clear
@ncamaa9 жыл бұрын
Isn't it much more likely that in the 3rd state, the Cl(-) will attack the H of the O(+) instead of the Carbonyl?
@niloofarnoormohammadi98983 жыл бұрын
Perfect👍
@asisable4 жыл бұрын
Thank you so much for sharing...❤️🙏🏾💯
@paysonbiker12 жыл бұрын
I'm confused; my o-chem prof 'actived' the oxygen from the carbonyl through resonance, and then used the subsequent, negatively charged oxygen as the nucleophilic site to attack the electrophilic sulfur site. The rest is basically the same and I end up with the correct product. Are both ways possible? Or is my professor wrong?
@quinnpuffer79016 ай бұрын
I've seen it done both ways
@TheCarnagekidd613 жыл бұрын
We can use dry PCl5 to change acetic acid to acetyl chloride as well?
@Acumen0611 жыл бұрын
yup, the explanation was clear but hopefully next time, aside from discussing the whole mechanism, the narrator could also discuss the state/phase of the beginning and end product, and the effect of the reaction, if it is endothermic, exothermic or toxic... i have a question sir, is it possible for this reaction to also form acetic anhydride? thanks
@callycap311 жыл бұрын
The mechanism is exactly the same. One of the Chlorine atoms from PCl5 acts first as a leaving group, then as a nucleophile, just in the same way as in this video.
@Ara20615 жыл бұрын
thank u.....thank u ....thank u ... *-*
@MrSmudger68713 жыл бұрын
@TheCarnagekidd6 - No problem
@thomaswilliams196312 жыл бұрын
Great vid...but good god the repeating is annoying...
@younismohamed62519 жыл бұрын
Why is oxalyl chloride a better reagent for the formation of acid chloride than thionyl sulfide?
@OsamaShehzad19957 жыл бұрын
whoever is watching this reaction, please do NOT follow it. This mechanism is completely WRONG according to fundamentals of organic chemistry. In the first step, lone pairs on Oxygen from (-OH) will NEVER attack in the presence of oxygen from carbonyl. but why? because if oxygen from carbonyl (C=O) attacks the chloride, the resulting intermediate can be resonance stabilized which cannot happen in case of attack from OH. Resonance stability shows that C=O oxygen remains more nucleophilic at all times
@sebastiancioban14765 жыл бұрын
Osama, can you help me with somenthing? I'm trying to find the radicals of dicarboxylic acids, like oxalic, succinic etc.., I know that there is 2 radicals (OC-CO and HOOC-CO), one of them is oxalyl for oxalic, but I don't know how to name the divalent RADICAL
@lizzyadeola6755 жыл бұрын
Why
@jdjdjdndn93696 жыл бұрын
Hi ✋ ... can I use HCl with carboxylic acid , if no why cannot use ?!
@MuhammadRafiMaulaAzmi10 ай бұрын
nicee
@55studebaker4 жыл бұрын
Your initial net rxn is shown as irreversible, but everything depicting the mechanism to the end is shown as in equilibrium. Don't get it.
@TheCarnagekidd613 жыл бұрын
@MrSmudger687 Thank you.
@zambrocca3 жыл бұрын
radical reaction??? are you sure?
@4SticksOfGum11 жыл бұрын
Does anyone know how you would form an acid chloride using PCl5?
@pranatipramanik1235 жыл бұрын
RCOOH+PCl5 ->RCOCl
@jhyland875 жыл бұрын
You repeat yourself quite a bit... repeat yourself quite a bit. :-P Great video tho! Question - Why am i having such a difficult time finding acetyl chloride (in the states)? I can't find it on Amazon or eBay. It doesn't appear to be on the list of chemicals the DEA restricts/watches... So i don't get why it's seemingly difficult to source.