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Organic chemistry
Course: Organic chemistry > Unit 3
Lesson 5: Functional groupsFunctional groups
An overview of some common functional groups.
Want to join the conversation?
- What was the bad joke? ☆(22 votes)
- It wasn’t a joke, but but a pun — a play on words that have the same sound but different meanings.
He said that you could remember that R-O-R is an ether (pronounced eether)) because it has an R group on either (pronounced eether) side.(75 votes)
- Are the functional groups set out in any order of priority? If not where can I find a list showing the priorities of the different functional groups?(14 votes)
- Yes, there is an order of priority for functional groups. You gan find a list at
http://www.masterorganicchemistry.com/2011/02/14/table-of-functional-group-priorities-for-nomenclature/(30 votes)
- Is water (H20) is also an ether?(9 votes)
- No. An ether must have two carbon atoms attached to the O atom.(18 votes)
- which is correct? 1-butene or but-1-ene?(7 votes)
- 1-butene is the older IUPAC nomenclature, whereas but-1-ene is the new format. Both are still acceptable for use, though the newer nomenclature will be standard in the near future. Hope this helped.(17 votes)
- isn't it suppose to be ethyl thiol instead of ethane thiol(10 votes)
- I looked at the IUPAC definitions, though somebody would easily understand if you said ethyl thiol, if you wanted to get really anal retentive: The suffix -thiol is added to the name of the alkane. This method is nearly identical to naming an alcohol and is used by the IUPAC. Example: CH3SH would be methanethiol (Wikipedia/IUPAC).(10 votes)
- Hi, ive just started learning about Organic Chemistry,Well I'm having trouble understanding functional groups and what does it do? Can I have a really basic explanation as I was basically clueless through the whole video, Thanks!!(4 votes)
- The basic explanation is in the beginning of the video: a functional group is a group of atoms that has predictable chemical behaviour. For example, alcohol groups are likely to engage in hydrogen bonding; thiol groups can form disulfide bonds; and aromatic rings have direct consequences for the light-absorptive behaviour of a compound. If we had to connect these recurrent chemical behaviours to random collections of atoms it would be difficult to find a pattern, and in fact, they connect to non-random collections of atoms. These non-random collections are called functional groups and if you want to continue learning organic chemistry it can be helpful to learn of few of them by heart.(13 votes)
- so the arene functional group, is that just also known as an aromatic ring AND a benzene or does the benzene have a specific characteristic that makes not all arenes benzenes?(3 votes)
- Right. There are many aromatic compounds. Benzene is just one of the aromatic compounds.(6 votes)
- does ethanol behaves like:
ACID OR ALKALI ?(2 votes)- it can behave like both depending on the other solvent/solute(4 votes)
- are arene and aIkene same?(1 vote)
- no - an alkene can have more than one double bond but only an arene has them arranged in an aromatic structure (usually a six C ring)(5 votes)
- Can an alkene have more than one double bonds?(2 votes)
- An allene is a carbon that is double bonded to two other carbons, if that's what you mean
https://en.wikipedia.org/wiki/Allene(3 votes)
Video transcript
- [Voiceover] A functional
group is a group of atoms that has a predictable chemical behavior. And there are many functional
groups in organic chemistry. And I'm gonna cover some
of the more common ones, the ones you'd have to
know for your class. So we start with an alkene. An alkene has a carbon-carbon
double bond in it, so here is a carbon-carbon double bond. R refers to the rest of the compound, or the remainder of the compound, and normally we're talking
about carbons and hydrogens. Let's look at an example of an alkene. So over here on the right we
can see that this molecule contains a carbon-carbon double
bond so this is an alkene. So how do we name this? Well if we had a four-carbon
alkane, let me go ahead and write out a four-carbon alkane here. So one, two, three, four,
we already know we should call that butane, so this
one should be called butane. And since we have a
four-carbon alkene, we're gonna lose our ending here
"a-n-e" and we're gonna add on "e-n-e", the ending for an alkene. So the name name of
this molecule is butene. I'm gonna go ahead and
write that out here. So this is butene. And if we number this
molecule, we start with the double bond and we
give this carbon right here a number one, and then we
have a number two right here, and a number three for this carbon, and a number four for this carbon. Our double bond starts at carbon one, so we put a one in front here
and we call this 1-butene. Let's look at another
example of an alkene. If we drew out a ring like this, we already know this
is called cyclohexane. If we put in a double
bond now it's cyclohexene. And you can see that
this has a carbon-carbon double bond and so does this molecule. So they both contain an
alkene functional group, and therefore both these molecules will undergo the same types of reactions. They have predictable chemical behaviors. And that's the usefulness of
grouping functional groups, of identifying functional
groups on molecules. Our next example of a
functional group is an alkyne. So this times it's a
carbon-carbon triple bond. Here you can see the carbon-carbon
triple bond in an alkyne. So if you look at the
right here's our example. And we number our carbons,
we can call this carbon one, this is carbon two, carbon three, and carbon four. So when you're drawing an alkyne we know that this is linear, this
portion of the molecule, this bond angle, is linear. So that's why it's drawn
in a straight line. So four carbons, so we would use "but", and we have a "y-n-e"
ending for an alkyne. So this is butyne, so let
me write out butyne here. And our triple-bond starts at carbon two, so here is where our triple-bond starts. So we could write 2-butyne
for the IUPAC name. Next we're looking at an arene, also called an aromatic ring,
and you're looking for this. You're looking for a six-carbon ring, and you have alternating
single-double bonds, so a total of three double bonds. Now just because it says double bonds, this doesn't mean it's
going to be an alkene. Actually arenes react in
different ways from alkenes and that's why this is a
separate functional group. So on the right here's
an example of an arene, or an aromatic ring, and this right here, this portion of the
molecule would be a benzene. So let's write out that, so benzene's a very famous organic chemistry molecule. And then we have a methyl group coming off of our benzene ring. So one name for this
would be methyl benzene. That's not the name you would usually see, normally you will hear this
molecule called toluene. So it's so common that
toluene is used most often. So toluene is an example of an arene. It contains an arene
functional group and so toluene would react in similar ways to benzene. Alright let's look at our
next functional group here. This is an alkyl halide, so
halide refers to halogen, so over here on the right
we have our halogen, so X could be a halogen
like chlorine or bromine. And R will be our alkyl group. For the example on the right, let me get a little more room down here,
our halogen is chlorine. And our alkyl group here
would be an ethyl group. We have a CH2 and a CH3. So one possible name for this molecule would be ethyl chloride. You could also call this
something like chloro ethane. Alright next functional
group is an alcohol. So an alcohol has an OH, an OH right here and an R for the rest of the molecule. As an example here's an
OH or a hydroxyl group, and then we have a CH2 and a CH3. So we have two carbons in this molecule, and we know two carbons is "eth". And for the full name
this would be ethanol. So a very famous molecule obviously. So this is ethanol. Next we have an ether. So an ether has an oxygen, with an R group on either side. So I'm sorry for the bad joke
but if it helps you remember that you have an R group on
either side of your oxygen, it's worth putting in a
bad joke into this video. So these R groups could
be the same R groups or they could be different R groups. For the example on the right we have R groups that happen to be the same. So here's our oxygen and here's an R group and here's an R group. Both of those R groups are ethyl groups. So we call this diethyl ether. So diethyl ether is the most famous ether. It's so famous that usually
it's just referred to as ether. But diethyl ether would be
one way to name this molecule. Next we're gonna look at a thiol. So a thiol is similar to an
alcohol, instead of an OH though we have an SH, so we have
sulfur instead of an oxygen. So for the example of a
thiol over here on the right, we have an SH here, then
we have an ethyl group. So one name for this
would be ethane thiol. So I'm gonna write this
out here, so "ethane thiol" is one possible name for this molecule. Next we have a sulfide. So a sulfide is similar to an
ether, remember for an ether we had R-O-R, for a sulfide we have R-S-R. So it's completely analogous to an ether. So on the right here's our
sulfur, and again we have two ethyl groups, so you can
call this diethyl sulfide. So let me write that out here, so this is "diethyl sulfide." And finally, for this video,
one more functional group. So this is an amine. So for this amine we have
nitrogen and then we have three R groups attached to nitrogen, or you could be talking
about hydrogens here. So any of these could
be hydrogens as well. So on the right is an example of an amine, we have a nitrogen with
a lone pair of electrons. This one has two ethyl groups
and one of our groups here is a hydrogen, so one name
for this is diethyl amine. Let me write out that one, so you could call this "diethyl amine." Alright, so we'll look at more functional groups in the next video.