The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given. Concept introduction: The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction. That means, R − B r forms R C H ( N H 3 + ) C O O −

Question

Want to see the full answer?

Answer 1

Question

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

What alkyl halide is used in the acetamidomalonic ester synthesis to preparea. lysine? b. phenylalanine?

22. The stability of carbocation can be accounted by which of the following structural effect? a. hyperconjugation b. inductive effect d. both a andb C. resonance 23. Secondary amines are more basic than primary amines because of what structural effect? a. hyperconjugation b. inductive effect C. resonance d. steric effect

show the esterification reaction between a. ethanoic acid and butanol b. propanoic acid and pentanol

Answer 2

Question

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Answer 6

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Answer 7

Chapter 21.6, Problem 23P

(a)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of lysine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Answer 8

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Answer 9

(b)

Interpretation Introduction

Interpretation:

The alkyl halide that used to synthesize of phenylalanine by acetamidomalonic ester synthesis has to be given.

Concept introduction:

The amino acid formed (R-group) from the acetamidomalonic (like N-phthalimidomalonic) ester synthesis is only depended upon the alkyl halide used in the reaction.

That means,

R−Br forms RCH(NH3+)COO−

Answer 10

Expert Solution & Answer

Answer 11

Expert Solution & Answer

Answer 12

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 13

Ch. 21.1 - a. Explain why, when the imidazole ring of...Ch. 21.2 - a. Which isomer(R)-alanine or (S)-alanineis...Ch. 21.2 - Prob. 4P Ch. 21.3 - Prob. 5P Ch. 21.3 - Prob. 6P Ch. 21.3 - Draw the predominant form for glutamate in a...Ch. 21.3 - a. Why is the pKa of the glutamate side chain...Ch. 21.4 - Calculate the pI of each of the following amino...Ch. 21.4 - a. Which amino acid has the lowest pI value? b....Ch. 21.4 - Prob. 12P

Concept explainers

Want to see the full answer?

Chapter 21 Solutions