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What functional group(s) is/are present [ the following compourd? Polnts)HO_NHCH;InitA chooUrondar ainde und 4nyamice and ccondaly akoholniute ed primary alcoholPim...

Question

What functional group(s) is/are present [ the following compourd? Polnts)HO_NHCH;InitA chooUrondar ainde und 4nyamice and ccondaly akoholniute ed primary alcoholPimary #corol end secondaty umine

What functional group(s) is/are present [ the following compourd? Polnts) HO_ NHCH; InitA choo Urondar ainde und 4ny amice and ccondaly akohol niute ed primary alcohol Pimary #corol end secondaty umine



Answers

Name the functional groups present in each of the following structures:

Let's identify name function groups in each of the following for a draw it out from the left hand side, we have a Harbach Selic acid. We have an aromatic ring which is die substituted. And we have a I dropped so good for be here. We haven't Esther. Chrissy here we have a he told here we have a Kobach Cilic acid. And for Dean, we have here we have and all the hype here we have an aromatic ring which is die substituted. And here we have a drugs.

Let's identify the functional groups in each of the following. For a gots three go upon oh, siege to seed two. Seed of about those three, uh, dysfunctional group here is a key tone and second function Group on the raid is also a key tone for be three ch two c o in HC H three functional group Right here is representative of a my for C green 03 c h Lots of functional groups in this one to in each C h three. So let's work away from left to rates. We have a hydroxy group. We haven't Esther. We have a try substituted aromatic ring. And we haven't Amy group and for d draw de out here each to see see double. But oh, each seen the whole he each to see. Uh, we have three groups here that are identical, and I'm going to circle them in here about these groups here on the right side. These air all car broke cilic acids and here got a I drop so good

Hi in this problem from the chapter organic chemistry we are given an organic compound has shown here we have to write the name of all functional groups present in the given molecule. So let's expand this molecule to see all the bonds. So this is HC double bond, oh ch two ch bonded to metal group C. H bonded to metal group C double born oh or H. So here we can see that in this compound to functional groups are present. This functional group represents L. D. Height functional group and the side it is suitable bone O. H. That is car box select acid function. So we can see that the functional groups present in the given molecule uh L. D. Hide and carb oxalic acid.

Right for our first compound. We have a pretty complex ring structure there. But if we were just looking at our functional groups, what we see is that we have O h attached up top and, oh, ages and alcohol. We see some ch three is there. Those were just methyl groups. So there's air. Carbon chains were not as focused on those when we talk about functional groups and then we also have a key toe, right? So a key tone is a double bonded oxygen and that is attached to a carbon I noticed there. There are no other oxygen's around it. If we change the number of oxygen's involved or if we didn't have just carbon attached, that would change the functional group. All right, on the next one, we have another alcohol. S 00 H is always an alcohol. This time we also have another oxygen involved. So up on the top, we see ah ch three so attached to the ring. Okay, so that ch 30 implies that it's just single bonds because the carbon has three other Hodgins attached to it. So any time that there is a single bottled oxygen in between two carbons gets an ether e T h e r. Right On the right hand side, we also have carbon double bonded toe oxygen and a single ball into a hydrogen gray with carbon. The chain on the other side. Any time you have that terminal double bonded. Oh, it's an elder hodge, right? So you gotta watch that. You gotta determine if it's attached to a carpet, just carbons or if there is a hydrogen there. If it's a terminal end substance, right, the big one that's last. We have quite a few functional groups here, so we see some new things. We see ah H to end attached to a carbon that's, Ah, classic N H two and H three compound that's called in a mean when it has a nitrogen there. Okay, inside. We also see we have a carbon double bonded to an oxygen, but it's important to know that there's a nitrogen also involved. Okay, so there are a lot of double bonded oxygen options, so when there's a nitrogen involved, we call it an amad. So it's a little bit different than in a mean because it does have the oxygen as well right up on the top. We have carbon double bonded to oxygen, single, bonded to oxygen as well, right? With carbon on either side of that whole complex. And that is an Esther. And then finally done on the bottom. We have a carbon double bonded to an oxygen with an O h. Remember that? Ohh. With a double bonded oxygen is a car box still like acid.


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