(a) Interpretation: The appearance of the high-resolution 13 C spectrum of (proton decoupled) methyl formate is to be stated. Concept introduction: The whole signals that appear in the proton decoupled 13 C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13 C − 13 C bond is that two 13 C atoms must be adjacent to each other. It is almost impossible for two 13 C nuclei to be adjacent to each other because the presence 13 C atoms in nature are less abundant and also the 13 C nuclei do not couple with the 12 C nuclei because of zero spin quantum number.

Question

Consider the reaction below and answer the following questions. Part 1 of 4 Br NaOCH2CH3 Identify the mechanisms involved. Check all that apply. SN 1 SN 2 E1 E2 None of the above Part 2 of 4 Skip Part Check esc F1 F2 lock 1 2 Q W A S #3 80 F3 F4 F5 F6 Save For © 2025 McGraw Hill LLC. All Rights Reserved. Terms ˇˇ % & 4 5 6 89 7 IK A 分 བ F7 F8 F9 F * E R T Y U 8 9 D F G H K V B N M 0 O

Answer 1

Question

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

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Consider the reaction below and answer the following questions. Part 1 of 4 Br NaOCH2CH3 Identify the mechanisms involved. Check all that apply. SN 1 SN 2 E1 E2 None of the above Part 2 of 4 Skip Part Check esc F1 F2 lock 1 2 Q W A S #3 80 F3 F4 F5 F6 Save For © 2025 McGraw Hill LLC. All Rights Reserved. Terms ˇˇ % & 4 5 6 89 7 IK A 分 བ F7 F8 F9 F * E R T Y U 8 9 D F G H K V B N M 0 O

What kind of holes are not generated when solid-state particles adopt a close packing pattern? Group of answer choices tetrahedral cubic octahedral None of the other choices are correct

For the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. 田 Major Product: Check ☐ + I Na OH esc F1 F2 2 1 @ 2 Q W tab A caps lock S #3 80 F3 69 4 σ F4 % 95 S Click and drag to sta drawing a structure mm Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use GO DII F5 F6 F7 F8 F9 F10 6 CO 89 & 7 LU E R T Y U 8* 9 0 D F G H J K L Z X C V B N M 36

Answer 2

Question

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

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Answer 3

Question

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

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Answer 4

Question

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

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Answer 5

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 6

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 7

Chapter 19, Problem 19.21QAP

Interpretation Introduction

(a)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) methyl formate is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are a singlet. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetaldehyde is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The appearance of the high-resolution 13C spectrum of (proton decoupled) acetone is to be stated.

Concept introduction:

The whole signals that appear in the proton decoupled 13C NMR spectrum are singlet in nature. Due to several reasons, the carbon atoms are do not coupled with the adjacent carbon atom. The only condition to form 13C−13C bond is that two 13C atoms must be adjacent to each other. It is almost impossible for two 13C nuclei to be adjacent to each other because the presence 13C atoms in nature are less abundant and also the 13C nuclei do not couple with the 12C nuclei because of zero spin quantum number.

Answer 12

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Ch. 19 - Prob. 19.1QAP Ch. 19 - Prob. 19.2QAP Ch. 19 - Prob. 19.3QAP Ch. 19 - Prob. 19.4QAP Ch. 19 - Prob. 19.5QAP Ch. 19 - A nucleus has a spin quantum number of 7/2. How...Ch. 19 - Prob. 19.7QAP Ch. 19 - Prob. 19.8QAP Ch. 19 - Prob. 19.9QAP Ch. 19 - Why is 133C-133C spin-spin splitting not observed...

Chapter 19 Solutions