Hi sir, thank you for the great video. Just wondering, in my textbook it says acyl chlorides react with ammonia to form an organic product and ammonium chloride rather than HCl. And also that acyl chlorides react with primary amines (e.g. methylamine) to form an organic product and i.e. methylammonium chloride rather than just HCl so I am a little confused Thanks again
Student 20 See this www.chemguide.co.uk/organicprops/acylchlorides/nitrogen.html#top If the ammonia is in excess, the HCl formed reacts with it to make the salt ammonium chloride
Brilliant video once again sir! However I dont understand the difference between phenyl groups and the benzene ring; at 3:30 i thought it would be benzyl ethanoate?
I think it's because when benzene is attached to a functional group like in the video, it changes from Benzyl (what you thought) to Phenyl. The same thing applies when a benzene bonds with an alkyl chain of 7 or more carbon atoms.
TheJassal98 The reactions of acid anhydride is exactly the same, forming the same products as acyl chloride but with the addition of a carboxylic acid.
Thank you. Explained in a simpler way compared to the book I have!
Cheers for that :)
Perfect timing - thanks so much! We have a test on this on Monday. 😭😭😭
a king here’s your crown 👑👑👑
i honestly love y so much thank u
Lara barznji How nice of you to say so. You’re welcome
Amazing video, I'm doing aqa and you've been so helpful. Btw do we need to know the mechanisms?
Hi sir, thank you for the great video.
Just wondering, in my textbook it says acyl chlorides react with ammonia to form an organic product and ammonium chloride rather than HCl. And also that acyl chlorides react with primary amines (e.g. methylamine) to form an organic product and i.e. methylammonium chloride rather than just HCl so I am a little confused
Thanks again
Had a question about the primary amides formation, what is the thing to do with forming a salt and NH4Cl?
Sir, in my book it says for the reaction of ethanoyl chloride + ammonia --> ethanamide + ammonium chloride
doesn't it form HCl or ammonium chloride?
Student 20 See this www.chemguide.co.uk/organicprops/acylchlorides/nitrogen.html#top If the ammonia is in excess, the HCl formed reacts with it to make the salt ammonium chloride
thank you very much sir :)
thanks a bunch
Do your tutorials cover all of the CIE syllabus?
Brilliant video once again sir! However I dont understand the difference between phenyl groups and the benzene ring; at 3:30 i thought it would be benzyl ethanoate?
Thanks! The benzyl group is C6H5CH2, phenyl is C6H5
I think it's because when benzene is attached to a functional group like in the video, it changes from Benzyl (what you thought) to Phenyl. The same thing applies when a benzene bonds with an alkyl chain of 7 or more carbon atoms.
Is there any acid anhydride videos?
TheJassal98 The reactions of acid anhydride is exactly the same, forming the same products as acyl chloride but with the addition of a carboxylic acid.
✊🏼✊🏼Thanks
6:28 , why can't the RCl be formed?
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do they give formulas on the data sheet lol..
kryptoNITE_ nope
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Too kind!
@@MaChemGuy💗💗💗💗
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