(a) Interpretation: How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any. Concept introduction: A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne ) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond. The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product. Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Question

The decomposition of dinitrogen pentoxide according to the equation: 50°C 2 N2O5(g) 4 NO2(g) + O2(g) follows first-order kinetics with a rate constant of 0.0065 s-1. If the initial concentration of N2O5 is 0.275 M, determine: the final concentration of N2O5 after 180 seconds. ...

Answer 1

Question

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

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The decomposition of dinitrogen pentoxide according to the equation: 50°C 2 N2O5(g) 4 NO2(g) + O2(g) follows first-order kinetics with a rate constant of 0.0065 s-1. If the initial concentration of N2O5 is 0.275 M, determine: the final concentration of N2O5 after 180 seconds. ...

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CS2(g) →CS(g) + S(g) The rate law is Rate = k[CS2] where k = 1.6 × 10−6 s−¹. S What is the concentration of CS2 after 5 hours if the initial concentration is 0.25 M?

Answer 2

Question

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

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Answer 3

Question

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

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Answer 4

Question

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

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Answer 5

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 6

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 7

Chapter 12, Problem 12.29P

Interpretation Introduction

(a)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown, along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 8

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 9

Interpretation Introduction

(b)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 10

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 11

Interpretation Introduction

(c)

Interpretation:

How the given compound with specified stereochemistry can be produced from an alkene is to be shown along with the reagents used and special conditions if any.

Concept introduction:

A cyclopropyl group can be introduced in a compound by reacting the corresponding alkene (or alkyne) with a carbene. A carbene is a species with only two groups, typically hydrogen or halogen atoms bonded to a carbon. The carbon atom also carries a lone pair of electrons or sometimes two unpaired electrons. This pair of electrons makes the carbene extremely reactive. Carbenes add to an alkene or alkyne by simultaneously forming bonds with the two carbon atoms from the double (or triple) bond. One bond is formed by the lone pair on the carbene and the other by the π bond pair from the initial double (or triple) bond.

The stereochemistry of the double bond is preserved in the reaction as it is a concerted addition. If the alkene has a cis configuration, the two similar substituents on the double bond end up on the same side of the cyclopropyl ring in the product. If it is a trans alkene, the similar substituents on the double bond end up on opposite sides of the ring in the product.

Carbenes are generated in situ, typically by irradiating a mixture of the alkene and diazomethane with UV light or by treating a mixture of the alkene and haloform (trihalomethane) with a strong base like an alkoxide.

Answer 12

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Answer 23

Ch. 12 - Prob. 12.1P Ch. 12 - Prob. 12.2P Ch. 12 - Prob. 12.3P Ch. 12 - Prob. 12.4P Ch. 12 - Prob. 12.5P Ch. 12 - Prob. 12.6P Ch. 12 - Prob. 12.7P Ch. 12 - Prob. 12.8P Ch. 12 - Prob. 12.9P Ch. 12 - Prob. 12.10P

Solution Summary: The author explains how a compound with specified stereochemistry can be produced from an alkene, along with the reagents used and special conditions if any.

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