The synthesis of bupropion from benzene and required inorganic reagents is to be devised. Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. The Lewis acid ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which reacts with benzene to form ketone . The reaction between a carbonyl compound with a halogen in acetic acid leads to the formation of α -halo carbonyl compound.

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 23, Problem 23.67P

Interpretation Introduction

Interpretation: The synthesis of bupropion from benzene and required inorganic reagents is to be devised.

Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. The Lewis acid ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which reacts with benzene to form ketone.

The reaction between a carbonyl compound with a halogen in acetic acid leads to the formation of α-halo carbonyl compound.

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 23, Problem 23.67P

Interpretation Introduction

Interpretation: The synthesis of bupropion from benzene and required inorganic reagents is to be devised.

Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. The Lewis acid ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which reacts with benzene to form ketone.

The reaction between a carbonyl compound with a halogen in acetic acid leads to the formation of α-halo carbonyl compound.

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Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 23, Problem 23.67P

Interpretation Introduction

Interpretation: The synthesis of bupropion from benzene and required inorganic reagents is to be devised.

Concept introduction: The Friedel-Craft acylation is a type of electrophilic substitution reaction. The Lewis acid ionizes the carbon-halogen bond of the acid chloride and forms a positively charged carbon electrophile which reacts with benzene to form ketone.

The reaction between a carbonyl compound with a halogen in acetic acid leads to the formation of α-halo carbonyl compound.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 23, Problem 23.67P

Interpretation Introduction