1. (a) Draw a three-dimensional line structure of (2Z,4R)-6-amino-3,4-dichloro-2-methylhex-2-enal. Place the aldehyde group on the right-hand side of your drawing. (b) Give the Cahn-Ingold-Prelog priority order of the four groups (-(CH2)2NH2, -H, -CI, -C4H4CIO) at the C4 stereocentre (Highest 1> 2 3 > 4 Lowest). 2. Study the curved arrows in the reactions below and provide structures of all the products that form for the given mechanistic step in the following reactions.

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter27: Amino Acids And Proteins
Section: Chapter Questions
Problem 27.39P: A chemically modified guanidino group is present in cimetidine (Tagamet), a widely prescribed drug...
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1. (a) Draw a three-dimensional line structure of (2Z,4R)-6-amino-3,4-dichloro-2-methylhex-2-enal. Place the aldehyde group on the
right-hand side of your drawing.
(b) Give the Cahn-Ingold-Prelog priority order of the four groups (-(CH2)2NH2, -H, -CI, -C4H4CIO) at the C4 stereocentre (Highest 1>2
> 3> 4 Lowest).
2. Study the curved arrows in the reactions below and provide structures of all the products that form for the given mechanistic step in
the following reactions.
(a)
Eto
(b)
Transcribed Image Text:1. (a) Draw a three-dimensional line structure of (2Z,4R)-6-amino-3,4-dichloro-2-methylhex-2-enal. Place the aldehyde group on the right-hand side of your drawing. (b) Give the Cahn-Ingold-Prelog priority order of the four groups (-(CH2)2NH2, -H, -CI, -C4H4CIO) at the C4 stereocentre (Highest 1>2 > 3> 4 Lowest). 2. Study the curved arrows in the reactions below and provide structures of all the products that form for the given mechanistic step in the following reactions. (a) Eto (b)
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