The method for preparation of 1-penten-3-one from 3-pentanone is given. Concept introduction: When the α-Bromo ketones can be dehydrobrominated by base treatment to yield α,Î² unsaturated ketones. For example, 2-methyl cyclohexanone gives 2-bromo-2-methylcyclohexanone on halogenation and the α bromo ketone gives 2-methyl-2-cyclohexanone when heated in pyridine. To give: The preparation method of1-penten-3-one from 3-pentanone is given.

Question

For this question, if the product is racemic, input both enantiomers in the same Marvin editor. A) Input the number that corresponds to the reagent which when added to (E)-but-2-ene will result in a racemic product. Input 1 for Cl, in the cold and dark Input 2 for Oy followed by H₂O, Zn Input 3 for D₂ with metal catalyst Input 4 for H₂ with metal catalyst B) Draw the skeletal structure of the major organic product made from the reagent in part A Marvin JS Help Edit drawing C) Draw the skeletal structure of the major organic product formed when (2)-but-2-ene is treated with peroxyacetic acid. Marvin 35 Help

Answer 1

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 22.3, Problem 5P

Interpretation Introduction

Interpretation:

The method for preparation of 1-penten-3-one from 3-pentanone is given.

Concept introduction:

When the α-Bromo ketones can be dehydrobrominated by base treatment to yield α,Î² unsaturated ketones. For example, 2-methyl cyclohexanone gives 2-bromo-2-methylcyclohexanone on halogenation and the α bromo ketone gives 2-methyl-2-cyclohexanone when heated in pyridine.

To give:

The preparation method of1-penten-3-one from 3-pentanone is given.

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For this question, if the product is racemic, input both enantiomers in the same Marvin editor. A) Input the number that corresponds to the reagent which when added to (E)-but-2-ene will result in a racemic product. Input 1 for Cl, in the cold and dark Input 2 for Oy followed by H₂O, Zn Input 3 for D₂ with metal catalyst Input 4 for H₂ with metal catalyst B) Draw the skeletal structure of the major organic product made from the reagent in part A Marvin JS Help Edit drawing C) Draw the skeletal structure of the major organic product formed when (2)-but-2-ene is treated with peroxyacetic acid. Marvin 35 Help

Michael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*

Rank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic. НОН НЬ OHd Онс

Answer 2

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 22.3, Problem 5P

Interpretation Introduction

Interpretation:

The method for preparation of 1-penten-3-one from 3-pentanone is given.

Concept introduction:

When the α-Bromo ketones can be dehydrobrominated by base treatment to yield α,Î² unsaturated ketones. For example, 2-methyl cyclohexanone gives 2-bromo-2-methylcyclohexanone on halogenation and the α bromo ketone gives 2-methyl-2-cyclohexanone when heated in pyridine.

To give:

The preparation method of1-penten-3-one from 3-pentanone is given.

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Check out sample textbook 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 22.3, Problem 5P

Interpretation Introduction

Interpretation:

The method for preparation of 1-penten-3-one from 3-pentanone is given.

Concept introduction:

When the α-Bromo ketones can be dehydrobrominated by base treatment to yield α,Î² unsaturated ketones. For example, 2-methyl cyclohexanone gives 2-bromo-2-methylcyclohexanone on halogenation and the α bromo ketone gives 2-methyl-2-cyclohexanone when heated in pyridine.

To give:

The preparation method of1-penten-3-one from 3-pentanone is given.

Expert Solution & Answer

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See solution

Check out sample textbook 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 22.3, Problem 5P

Interpretation Introduction