Carboxylic acid derivatives - amides, anhydrides, esters and acyl chlorides. Created by Sal Khan.
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- This question is not directly from the video. If a compound, which has an amine group and a hydroxyl group, is made to react with an acid, what will be the product? Will it be an amide or an ester??(1 vote)
- The product will be an ester. The acid will protonate the amine and convert it to a substituted ammonium ion, which cannot act as a nucleophile.(5 votes)
- 2:14... the IUPAC name is ethanamide, but where does this name indicate that it is an amine group attached specifically to an acyl group? I don't see the acyl "-oic" anywhere. This just sounds like ethane bonded to an amine group (which it isn't).(1 vote)
- If the compound were ethylamine, the IUPAC name would be ethanamine. The suffix "amine" tells you that the compound is an amine.
In ethanamide, the suffix "amide" tells you that you have an amide group, that is, a C=O attached to an N atom. So "ethanamide" tells you that you have a two-carbon chain that includes a C=O attached to an N atom, i.e., CH3CONH2.
The general rule for naming amides is that you replace the ending "oic acid" of the acid name with the ending "amide". So ethanoic acid becomes ethanamide.(3 votes)
- How do we name anhydrides present in a cyclic system?(1 vote)
- No difference. We simply replace the word "acid" in the name of the acid with the word "anhydride". Thus, the anhydride formed from cyclobutane-1,2-dicarboxylic acid is called cyclobutane-1,2-dicarboxylic anhydride.(2 votes)
- Hello, I just was wondering about the explanation you give to us related to how to name esters at approximately4:00, I think the explanation is not complete because you do not mention how to name the methyl group attached to the oxygen. Thank you.(1 vote)
- What's the difference between carbonyl group and acyl group...?(0 votes)
- A carbonyl group is just a C=O group. An acyl group is an R-C=O group. That is, it has a carbon atom directly attached to the carbonyl carbon.(3 votes)
- Would peroxylic acid also be a carboxylic acid derivative, or does it not occur naturally that much so its irellevant(1 vote)
- there is a mistake in the esters naming part ,
starting from3:50(1 vote)
- Technically, you are correct. The ester shown is an acetate or ethanoate, but the name of this particular ester is methyl acetate or methyl ethanoate.(1 vote)
- At about3:10Sal names part of the molecule 'propan' but surely that isnt mentioning the oxygen atom which is on it? Shouldnt it be something more like N-methyl propanoic amide???(1 vote)
- Don't forget that at the base of a carbonyl there is another carbon. Even though it looks like the double bond is just going to the oxygen, there is still a carbon there at the base of the double bond, which means that it would have three carbons on the left side of the molecule and therefore would be named as 'propan'. Hope this helps!(1 vote)
- at3:00,the given structure have a secondary nitrogen or not(0 votes)
- Yes, the N atom is secondary. There are two different ways of classifying amides. One way is the primary, secondary, tertiary system. In a primary amide, the N atom is bound to one carbon – the carbonyl carbon. Successive substitutions of the amino H atoms by carbon atoms turn the amide into secondary and tertiary amides.
The more common way is to describe amides as unsubstituted, monosubstituted, or disubstituted, according to the number of alkyl or aryl substituents on the N atom.
Thus, N-methylpropanamide is a monosubstituted amide with a 2° N atom.(3 votes)
What I want to do in this video is talk about a bunch of molecules or classes of molecules that can be derived from carboxylic acid. And just to show a specific example I'll show things that can be derived from acetic acid. And just as a review, acetic acid looks like this. The common name, as I just said, is acetic acid, and if you want to use the systematic name, you look for the longest chain, which is right over there. There's two carbons. So we use the eth- prefix, so it's ethan-, and since this is a carboxylic acid, it is ethanoic acid. Now, the derivatives of acetic acid, and we can later generalize this to all carboxylic acids. We really just have to change what's going on in this carbon chain right here. It won't have to necessarily just be two carbons. It can just keep going. It could have benzene rings, whatever, and that would change the name. But really, I just want to give you the gist and the gist of the naming. So if we were to replace this hydroxyl group with an amine, and in future videos we'll see how that is done, so let me just draw the acyl group. So the acyl group is just that right over there. And we're just going to keep changing what's bonded to the acyl group right over here. So if this is bonded to an amine, so let me draw-- well, this would be the simplest amine right over here, which would be NH2. This thing right here it's called an amide, and if we were to give this its common name, it would be acetamide. This particular example would be acetamide. And if we wanted the systematic name for it, it would be ethanamide. You have two carbons right there so it is ethanamide. Now the natural question is, all amines won't just be primary, you might have other things other than hydrogens attached to it, other radical groups, other carbon chains, so how do you name those? And so if you had a molecule that looked like this, and actually, let me just change things up a little bit so that we diverge a little bit from the ethane route. So let's say you had three carbons bonded or part of the acyl group right there. And then, we are bonded to a nitrogen, which is bonded to a methyl group and then another hydrogen. In this case, you start naming with this methyl group right here and to show that that methyl group is attached to the nitrogen, you call this N-methyl. And then you look at the chain that forms the acyl group, the carbon chain. We have one, two, three carbons so it is propanamide. If you had another methyl here you would say N comma N-dimethyl. If you had a methyl here and a propyl group here, you would've called it N-methyl-N-propyl-propanamide. So hopefully that gives you a sense of amides. Now, and this is something we've seen before so it's a little bit of review, if you have something that looks like this, I'll have it attached to a methyl group right over here. We've seen this before. This is an ester. And if we have an-- let me actually make the part that makes it an ester in blue to diferentiate it. We keep substituting what is attached to the acyl group. Let me label it. This right here is called an acyl group. That right there is an acyl group. So right over here, for the ester, if we were to give it its common name, and we've seen this ester before, it is acetate. And if we wanted to give it its systematic , name you look at the longest chain, one, two carbons so it is ethan-- and you don't call it ethanoic acid anymore. You call it ethanoate, just like that. Now, the next one, and we haven't seen this one before, and it looks complex, but when you really break it down into its constituents, it's not so bad. So let's say we have a molecule that looks like this. So we have one acyl group bonded to an oxygen, which is bonded to another acyl group. So it's almost like you have two carboxylic acids that have been joined together. And you really do have two acyl groups joined by an oxygen here. This is called an anhydride. And they look very complex, but you just have to realize they're two carboxylic acids attached to each other and usually the same one. Most anhydrides you're going to see in organic chemistry are formed from the same carboxylic acid, so how ever many carbons you have on this end, you're normally going to have on this end. So the way the name these is you name it just the same way that you would have named the carboxylic acid, but instead of writing the word acid, you write the word anhydride. So this right here would be acetic anhydride. It's derived from acetic acid. This right here is acetic anhydride. Or the systematic name is, we have one, two carbons so it's ethanoic anhydride. And just to make things clear, if this molecule instead of that, if we had something that looked like this, where the carbons chains on either end had three carbons. One, two, three, one, two, three. We would call this propanoic anhydride. In the unusual circumstance, and it is unusual, where you would see different carbon chains here, you would list each of them. So if this had two here and three here, it would be ethanoic propanoic anhydride. But that is very, very unusual. Normally, these carbon chains on either end of-- or both acyl will groups will contain the same number of carbons. Now, the last carboxylic acid derivative that you should know about, and we've already seen it, are the acyl halides, and, in particular, the acyl chlorides. So let me draw it right over here. So you have your acyl group right there and then it is bonded to a chlorine and this right here is an acyl chloride, maybe the most intuitive name. This right here is an acyl group and then you have a chlorine, so it's an acyl chloride. And we've seen this exact acyl chloride. It's derived from acetic acid, so this is acetyl chloride. But if you wanted to give it its systematic name, and we haven't seen it's systematic name before, we have one, two carbons so it is ethanoyl. This tells us that we are dealing with an acyl group. Ethanoyl chloride is how we would name this. And if this had three carbons, it would be propanoyl chloride. So, hopefully, that gives you at least a good introduction to the differences in structures of all these groups and an introduction to naming them. In the next video, we'll talk a little bit about the relative stabilities and then it'll give you good intuition on which direction a reaction might go. Are you more likely to go from amide to an acyl chloride or from an acyl chloride to an amide or anything in between?