Try it on paper first. A hint, the key idea and the worked solution are here when you need them.
Give the IUPAC name of each compound.
The carboxyl carbon is carbon 1. Acids come from oxidation of primary alcohols, aldehydes and alkylbenzenes (a benzylic hydrogen is needed), from hydrolysis of nitriles, amides and esters, and from RMgX with CO, which adds one carbon. Two hydrogen bonds join acid molecules in a dimer, so the molar mass found in benzene is near double.
Have you tried it?
Work it out on paper first. It is fine to get stuck or make a mistake: that is how we learn. When you are ready, go through the solution one step at a time, and check each step against your own.
Step 1. Four carbons with a methyl on carbon 2: 2-methylbutanoic acid.
Step 2. Five carbons with a COOH at each end: pentanedioic acid, also called glutaric acid.
Step 3. A phenyl group on carbon 2 of a two-carbon acid: 2-phenylethanoic acid, also called phenylacetic acid.
Step 4. A hydroxyl group on carbon 2 of a three-carbon acid: 2-hydroxypropanoic acid, lactic acid.
Step 5. Chlorine on carbon 3: 3-chloropropanoic acid.
Step 6. A double bond from carbon 2: prop-2-enoic acid, acrylic acid.
Step 7. Five carbons, no branches: pentanoic acid, valeric acid.
Step 8. Three carbons with two COOH groups: propanedioic acid, malonic acid.
Check. The carboxyl carbon is always carbon 1, and no number is needed for it.
Log in to join the discussion.
Loading…