The aldehyde as an intermediate formed in the reduction of ethyl benzoate with lithium aluminum hydride has to be stated. Concept introduction: Oxidation reaction involves increase in the C − X bonds (where X usually is oxygen or a halogen atom) or decrease in the C − H bonds. Reduction reaction involves decrease in the C − X bonds (where X usually is oxygen or a halogen atom) or increase in the C − H bonds. In electrophilic aromatic substitution, if the ring bears several substituents, then the orientation is controlled by the most activating substituent.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 20.11, Problem 16P

Interpretation Introduction

Interpretation:

The aldehyde as an intermediate formed in the reduction of ethyl benzoate with lithium aluminum hydride has to be stated.

Concept introduction:

Oxidation reaction involves increase in the C−X bonds (where X usually is oxygen or a halogen atom) or decrease in the C−H bonds.

Reduction reaction involves decrease in the C−X bonds (where X usually is oxygen or a halogen atom) or increase in the C−H bonds.

In electrophilic aromatic substitution, if the ring bears several substituents, then the orientation is controlled by the most activating substituent.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Give the organic product: O A O B Ос ○ D -NH–CH3 + CH3 CH3 NEN C ? A CH3 CH3 NH- CH3 B CH3 CH3 N=N- C CH3 CH3 N=NNH CH3 D CH3 N=N CH3 NHCH3 LNH CHO

Finish the reaction- hand written please

Give the organic products: (benzyne) Br ? CH3 + K* :NH, liq NH3 HINT: Two products are formed. Each is a substituted aniline; they are isomers of each other. NH2 II I H₂N. CH3 CH3 III Select one: ○ A. I and II ○ B. I and III O C. I and IV O D. II and III O E. III and IV H₂N CH3 IV CH₂-NH2

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 20.11, Problem 16P

Interpretation Introduction

Interpretation:

The aldehyde as an intermediate formed in the reduction of ethyl benzoate with lithium aluminum hydride has to be stated.

Concept introduction:

Oxidation reaction involves increase in the C−X bonds (where X usually is oxygen or a halogen atom) or decrease in the C−H bonds.

Reduction reaction involves decrease in the C−X bonds (where X usually is oxygen or a halogen atom) or increase in the C−H bonds.

In electrophilic aromatic substitution, if the ring bears several substituents, then the orientation is controlled by the most activating substituent.

Expert Solution & Answer

Want to see the full answer?

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 aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 20.11, Problem 16P

Interpretation Introduction

Interpretation:

The aldehyde as an intermediate formed in the reduction of ethyl benzoate with lithium aluminum hydride has to be stated.

Concept introduction:

Oxidation reaction involves increase in the C−X bonds (where X usually is oxygen or a halogen atom) or decrease in the C−H bonds.

Reduction reaction involves decrease in the C−X bonds (where X usually is oxygen or a halogen atom) or increase in the C−H bonds.

In electrophilic aromatic substitution, if the ring bears several substituents, then the orientation is controlled by the most activating substituent.

Expert Solution & Answer

Want to see the full answer?

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 aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 20.11, Problem 16P

Interpretation Introduction