What amino acid has an aromatic ring in its side chain?
Well... more than one, that's for sure. You have Tyrosine, Phenylalanine, and Tryptophan.
Notice how all three of those have conjugated pi orbital systems in their sidechains. The benzene ring is a good hint as to whether or not their sidechains have an aromatic ring---benzene is the most basic model for aromaticity!
From there, you might ask yourself, "is the rest of the sidechain conjugated?" Try drawing the resonance structure of Tryptophan, starting at the NH lone pair, going counterclockwise. You should end up on the left carbon on the upper-right double bond on benzene. CHALLENGE: Does Tryptophan have any conservative mutations? That is, are there any amino acids similar enough to take its place and perform its function? Assume the mutation is only between the known 20 amino acids (Ala, Cys, Asp, Glu, Phe, Gly, His, Ile, Lys, Leu, Met, Asn, Pro, Gln, Arg, Ser, Thr, Val, Trp, Tyr).
By signing up, you agree to our Terms of Service and Privacy Policy
The amino acid with an aromatic ring in its side chain is phenylalanine.
By signing up, you agree to our Terms of Service and Privacy Policy
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- What do the functional groups determine?
- Why are functional groups important?
- What makes a cycloalkane different from other alkanes?
- How can I draw the following ethers: 1-propoxypentane, 2-ethoxybutane, 1-methoxy-4-chlorohexane, and 3-butoxy-2,4-dimethyloctane?
- What is the mechanism of the reaction of NaI in acetone with an alkyl halide?
- 98% accuracy study help
- Covers math, physics, chemistry, biology, and more
- Step-by-step, in-depth guides
- Readily available 24/7