The products, when HgSO 4 / H 2 SO 4 catalysed hydration and hydroboration-oxidation are applied to hex − 1 − yne . Interpretation: The products, when HgSO 4 / H 2 SO 4 catalysed hydration and hydroboration-oxidation are applied to hex − 1 − yne to be shown. Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water. An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

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 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Potential Energy (kJ) 1. Consider these three reactions as the elementary steps in the mechanism for a chemical reaction. AH = -950 kJ AH = 575 kJ (i) Cl₂ (g) + Pt (s) 2C1 (g) + Pt (s) Ea = 1550 kJ (ii) Cl (g)+ CO (g) + Pt (s) → CICO (g) + Pt (s) (iii) Cl (g) + CICO (g) → Cl₂CO (g) Ea = 2240 kJ Ea = 2350 kJ AH = -825 kJ 2600 2400 2200 2000 1800 1600 1400 1200 1000 a. Draw the potential energy diagram for the reaction. Label the data points for clarity. The potential energy of the reactants is 600 kJ 800 600 400 200 0 -200- -400 -600- -800- Reaction Progress

Can u help me figure out the reaction mechanisms for these, idk where to even start

Hi, I need your help with the drawing, please. I have attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!

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 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

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 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

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 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 6

Chapter 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 7

Chapter 9.9F, Problem 9.21P

(a)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−1−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 8

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 9

(b)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−2−yne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 10

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 11

(c)

Interpretation Introduction

To determine: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to hex−3−yne.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 12

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 13

(d)

Interpretation Introduction

To determine: The product, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne.

Interpretation: The products, when HgSO4/H2SO4 catalysed hydration and hydroboration-oxidation are applied to cyclodecyne to be shown.

Concept introduction: Hydroboration-oxidation reactions convert an alkyne molecule in to ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the two step mechanism, whereas an alkene molecule in hydroboration-oxidation reaction is converted into alcohol by the addition of water.

An acid catalysed hydration reaction of alkynes in the presence of mercuric sulphate gives ketone.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 9.1 - a. Count the elements of unsaturation in...Ch. 9.2 - Prob. 9.2P Ch. 9.4B - What reaction would acetylene likely undergo if it...Ch. 9.6 - Prob. 9.4P Ch. 9.6 - Predict the products of the following acid-base...Ch. 9.7A - Solved Problem9-1 showed the synthesis of...Ch. 9.7A - Show how you might synthesize the following...Ch. 9.7B - Prob. 9.8P Ch. 9.7B - Show how you would synthesize...Ch. 9.8 - When 2,2-dibromo-1-phenylpropane is heated...

Solution Summary: The author explains how hydroboration-oxidation reactions convert an alkyne molecule into ketone or aldehyde in the presence of disiamylborane and hydrogen peroxide through the

Concept explainers

Want to see the full answer?

Chapter 9 Solutions