(a) Interpretation: The structure of the salmeterol should be drawn. Concept Introduction: Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H 2 gas and Pd as catalyst and produce respective alcohols.

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Answer 1

Question

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

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1. Calculate the accurate monoisotopic mass (using all 1H, 12C, 14N, 160 and 35CI) for your product using the table in your lab manual. Don't include the Cl, since you should only have [M+H]*. Compare this to the value you see on the LC-MS printout. How much different are they? 2. There are four isotopic peaks for the [M+H]* ion at m/z 240, 241, 242 and 243. For one point of extra credit, explain what each of these is and why they are present. 3. There is a fragment ion at m/z 184. For one point of extra credit, identify this fragment and confirm by calculating the accurate monoisotopic mass. 4. The UV spectrum is also at the bottom of your printout. For one point of extra credit, look up the UV spectrum of bupropion on Google Images and compare to your spectrum. Do they match? Cite your source. 5. For most of you, there will be a second chromatographic peak whose m/z is 74 (to a round number). For one point of extra credit, see if you can identify this molecule as well and confirm by…

Please draw, not just describe!

can you draw each step on a piece of a paper please this is very confusing to me

Answer 2

Question

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Expert Solution & Answer

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Check out a sample textbook solution

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Answer 3

Question

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Expert Solution & Answer

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Check out a sample textbook solution

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Answer 5

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Answer 6

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Answer 7

Chapter 16, Problem 82P

Interpretation Introduction

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

Answer 8

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Answer 9

Interpretation Introduction

(b)

Interpretation:

One chirality center in a salmeterol molecule should be identified.

Concept Introduction:

Chirality is the presence of an asymmetric carbon center in a molecule and a molecule which contains a chiral center cannot superimpose on its mirror image. To consider as chiral, molecule or object and its mirror image should not superimpose. To consider as achiral, molecule or object and its mirror image should be superimposed with each other.

In the above diagram, where C is the chiral center/ asymmetric carbon center.

A, B, D, E are four different functional groups.

Answer 10

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Answer 11

Interpretation Introduction

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Answer 12

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Answer 13

Expert Solution & Answer

Answer 14

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Answer 15

Ch. 16.1 - Prob. 16.1P Ch. 16.1 - Draw the structure of the three constitutional...Ch. 16.2 - Give the IUPAC name for each aldehyde. a. (...Ch. 16.2 - Give the structure corresponding to each TUPAC...Ch. 16.2 - Prob. 16.4P Ch. 16.2 - Prob. 16.2PP Ch. 16.2 - Give the structure corresponding to each name. a....Ch. 16.3 - Which compound in each pair has the higher boiling...Ch. 16.3 - Acetone and progesterone are two ketones that...Ch. 16.4 - Prob. 16.8P

(a) Interpretation: The structure of the salmeterol should be drawn. Concept Introduction: Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H 2 gas and Pd as catalyst and produce respective alcohols.

Solution Summary: The author explains that the structure of salmeterol should be drawn. Chirality is the presence of an asymmetric carbon center in the molecule.

Concept explainers

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

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Chapter 16 Solutions

(a) Interpretation: The structure of the salmeterol should be drawn. Concept Introduction: Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H 2 gas and Pd as catalyst and produce respective alcohols.

Solution Summary: The author explains that the structure of salmeterol should be drawn. Chirality is the presence of an asymmetric carbon center in the molecule.

Concept explainers

(a) Interpretation: The structure of the salmeterol should be drawn. Concept Introduction: Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

(c) Interpretation: Enantiomers of salmeterol in three dimensions should be drawn. Concept Introduction: Mirror image of a molecule is a reflected duplicate of the molecule. Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.

Want to see the full answer?

Chapter 16 Solutions

(a)

Interpretation:

The structure of the salmeterol should be drawn.

Concept Introduction:

Aldehydes and ketones which are considered as carbonyl compounds, undergo reduction reactions in the presence of H2 gas and Pd as catalyst and produce respective alcohols.

(c)

Interpretation:

Enantiomers of salmeterol in three dimensions should be drawn.

Concept Introduction:

Mirror image of a molecule is a reflected duplicate of the molecule.

Enantiomers − the mirror image of the original molecule of a chiral molecule. These are stereoisomers.