(a) Interpretation: The structural formula of 2-aminopropanoic acid should be drawn. Concept Introduction: One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

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Answer 1

Question

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

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5. A solution of sucrose is fermented in a vessel until the evolution of CO2 ceases. Then, the product solution is analyzed and found to contain, 45% ethanol; 5% acetic acid; and 15% glycerin by weight. If the original charge is 500 kg, evaluate; e. The ratio of sucrose to water in the original charge (wt/wt). f. Moles of CO2 evolved. g. Maximum possible amount of ethanol that could be formed. h. Conversion efficiency. i. Per cent excess of excess reactant. Reactions: Inversion reaction: C12H22O11 + H2O →2C6H12O6 Fermentation reaction: C6H12O6 →→2C2H5OH + 2CO2 Formation of acetic acid and glycerin: C6H12O6 + C2H5OH + H₂O→ CH3COOH + 2C3H8O3

Show work. don't give Ai generated solution. How many carbons and hydrogens are in the structure?

13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. cleavage Bond A •CH3 + 26.← Cleavage 2°C. + Bond C +3°C• CH3 2C Cleavage E 2°C. 26. weakest bond Intact molecule Strongest 3°C 20. Gund Largest argest a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. C Weakest bond A Produces Most Bond Strongest Bond Strongest Gund produces least stable radicals Weakest Stable radical b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 13°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. • CH3 methyl radical Formed in Gund A Cleavage c.…

Answer 2

Question

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

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Answer 3

Question

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

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Answer 4

Question

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

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Answer 5

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

Answer 6

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Answer 7

Chapter 17, Problem 7P

Interpretation Introduction

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

Answer 12

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

Answer 13

Interpretation Introduction

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

Answer 14

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Answer 15

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Answer 16

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Answer 17

Ch. 17.2 - Prob. 17.1QC Ch. 17.5 - Prob. 17.2QC Ch. 17.5 - Prob. 17.3QC Ch. 17 - 18-4 Answer true or false. (a) The functional...Ch. 17 - Prob. 2P Ch. 17 - 18-6 Name and draw structural formulas for the...Ch. 17 - 18-7 Write the IUPAC name for each carboxylic...Ch. 17 - 18-8 Write the IUPAC name for each carboxylic...Ch. 17 - Prob. 6P Ch. 17 - Prob. 7P

(a) Interpretation: The structural formula of 2-aminopropanoic acid should be drawn. Concept Introduction: One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Solution Summary: The author explains the structural formula of 2-aminopropanoic acid and the structure of 3-dinitrobenzoic acid.

Concept explainers

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

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Chapter 17 Solutions

(a) Interpretation: The structural formula of 2-aminopropanoic acid should be drawn. Concept Introduction: One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

Solution Summary: The author explains the structural formula of 2-aminopropanoic acid and the structure of 3-dinitrobenzoic acid.

Concept explainers

(a) Interpretation: The structural formula of 2-aminopropanoic acid should be drawn. Concept Introduction: One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

(b) Interpretation: The structural formula of 3, 5-dinitrobenzoic acid should be drawn. Concept Introduction: Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

(c) Interpretation: The structural formula of dichloroacetic acid should be drawn. Concept Introduction: Two of the hydrogens of acetic acid are replaced by two chloro groups.

(d) Interpretation: The structural formula of o-aminobenzoic acid should be drawn. Concept Introduction: Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.

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Chapter 17 Solutions

(a)

Interpretation:

The structural formula of 2-aminopropanoic acid should be drawn.

Concept Introduction:

One of the hydrogen of propanoic acid at carbon 2 position is replaced by amino group.

(b)

Interpretation:

The structural formula of 3, 5-dinitrobenzoic acid should be drawn.

Concept Introduction:

Two nitro groups are at position 3 and 5 with respect to benzoic acid which is at carbon 1.

(c)

Interpretation:

The structural formula of dichloroacetic acid should be drawn.

Concept Introduction:

Two of the hydrogens of acetic acid are replaced by two chloro groups.

(d)

Interpretation:

The structural formula of o-aminobenzoic acid should be drawn.

Concept Introduction:

Ortho (o) position is the C-2 and C-6 position with respect to the major functional group in benzene system.