(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.

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achieve.macmillanlearning.com Canvas EA eac h Hulu YouTube G 3 methyl cyclobutanol - Google Search Ranking Phenol Acidity Course -236 - Organic Chemistry - Mac... ← Assessment Completed 10 of 22 Questions 1 + Netflix paramount plus chem hw Galdehyde reaction with grignard reagent... b My Questions | bartleby M Inbox - chenteislegit@gmail.com - Gmail Due: Fri, Jan 31 Resources Solution Penalized ? Hint Submit Answer Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the reactions.) Route 1 Aldehyde 1 or +98 Aldehyde 2 Route 2 Q6 +100 Solved in 1 attempt Q7 +95 Solved in 2 attempts Q8 +98 Unlimited attempts possible + + Grignard 1 OH H3O+ Grignard 2 Answer Bank Q9 +90 MgBr Unlimited attempts possible CH3CH2CH2MgBr Q10 Unlimited attempts Q11 ? ? +100 in 1 attempt 2-methyl-3-hexanol CH3CH2MgBr H H о H Attempt 3

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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achieve.macmillanlearning.com Canvas EA eac h Hulu YouTube G 3 methyl cyclobutanol - Google Search Ranking Phenol Acidity Course -236 - Organic Chemistry - Mac... ← Assessment Completed 10 of 22 Questions 1 + Netflix paramount plus chem hw Galdehyde reaction with grignard reagent... b My Questions | bartleby M Inbox - chenteislegit@gmail.com - Gmail Due: Fri, Jan 31 Resources Solution Penalized ? Hint Submit Answer Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the reactions.) Route 1 Aldehyde 1 or +98 Aldehyde 2 Route 2 Q6 +100 Solved in 1 attempt Q7 +95 Solved in 2 attempts Q8 +98 Unlimited attempts possible + + Grignard 1 OH H3O+ Grignard 2 Answer Bank Q9 +90 MgBr Unlimited attempts possible CH3CH2CH2MgBr Q10 Unlimited attempts Q11 ? ? +100 in 1 attempt 2-methyl-3-hexanol CH3CH2MgBr H H о H Attempt 3

2) (4 pt) After the reaction was completed, the student collected the following data. Crude product data is the data collected after the reaction is finished, but before the product is purified. "Pure" product data is the data collected after attempted purification using recrystallization. Student B's data: Crude product data "Pure" product data after recrystallization Crude mass: 0.93 g grey solid Crude mp: 96-106 °C Crude % yield: Pure mass: 0.39 g white solid Pure mp: 111-113 °C Pure % yield: a) Calculate the crude and pure percent yields for the student's reaction. b) Summarize what is indicated by the crude and pure melting points.

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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