The mechanism for the reaction in which a secondary nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid is to be drawn. Concept introduction: The nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid. The nitro group is an electron withdrawing group. Acidity of the alpha C-H turns the nitro group into good leaving group via proton transfer steps. This reaction is conducted in acidic medium, that is, in the presence of aqueous sulfuric acid. Under this condition, water acts as a nucleophile, and nucleophilic addition takes place at alpha carbon. Then, after proton transfer steps, the electron withdrawing group turns into a good leaving group, which leads to formation of a ketone.

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Answer 1

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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 18, Problem 18.83P

Interpretation Introduction

Interpretation:

The mechanism for the reaction in which a secondary nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid is to be drawn.

Concept introduction:

The nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid. The nitro group is an electron withdrawing group. Acidity of the alpha C-H turns the nitro group into good leaving group via proton transfer steps. This reaction is conducted in acidic medium, that is, in the presence of aqueous sulfuric acid. Under this condition, water acts as a nucleophile, and nucleophilic addition takes place at alpha carbon. Then, after proton transfer steps, the electron withdrawing group turns into a good leaving group, which leads to formation of a ketone.

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Deducing the reactants of a Diels-Alder reaction n the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ • If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Explanation Check Click and drag to start drawing a structure. >

Predict the major products of the following organic reaction: + Some important notes: A ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure.

if the answer is no reaction than state that and please hand draw!

Answer 2

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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 18, Problem 18.83P

Interpretation Introduction

Interpretation:

The mechanism for the reaction in which a secondary nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid is to be drawn.

Concept introduction:

The nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid. The nitro group is an electron withdrawing group. Acidity of the alpha C-H turns the nitro group into good leaving group via proton transfer steps. This reaction is conducted in acidic medium, that is, in the presence of aqueous sulfuric acid. Under this condition, water acts as a nucleophile, and nucleophilic addition takes place at alpha carbon. Then, after proton transfer steps, the electron withdrawing group turns into a good leaving group, which leads to formation of a ketone.

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Answer 3

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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 18, Problem 18.83P

Interpretation Introduction

Interpretation:

The mechanism for the reaction in which a secondary nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid is to be drawn.

Concept introduction:

The nitro group can be hydrolyzed to a ketone on treatment with aqueous sulfuric acid. The nitro group is an electron withdrawing group. Acidity of the alpha C-H turns the nitro group into good leaving group via proton transfer steps. This reaction is conducted in acidic medium, that is, in the presence of aqueous sulfuric acid. Under this condition, water acts as a nucleophile, and nucleophilic addition takes place at alpha carbon. Then, after proton transfer steps, the electron withdrawing group turns into a good leaving group, which leads to formation of a ketone.

Expert Solution & Answer

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Check out a sample textbook solution

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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 18, Problem 18.83P

Interpretation Introduction