ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<
ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<
5th Edition
ISBN: 9781260293685
Author: SMITH
Publisher: MCGRAW-HILL CUSTOM PUBLISHING
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Chapter 11, Problem 11.36P

What alkynes give each of the following ketones as the only product after hydration with H 2 O , H 2 SO 4 and HgSO 4 .

a. Chapter 11, Problem 11.36P, 11.36 What alkynes give each of the following ketones as the only product after hydration with ,  , example  1 bChapter 11, Problem 11.36P, 11.36 What alkynes give each of the following ketones as the only product after hydration with ,  , example  2. c. Chapter 11, Problem 11.36P, 11.36 What alkynes give each of the following ketones as the only product after hydration with ,  , example  3 d. Chapter 11, Problem 11.36P, 11.36 What alkynes give each of the following ketones as the only product after hydration with ,  , example  4

Expert Solution
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Interpretation Introduction

(a)

Interpretation: The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are to be predicted.

Concept introduction: A terminal alkyne reacts with H2O, H2SO4 (strong acid) and HgSO4 to form a ketone. In this case, hydrogen atom and OH will get attach to the less substituted carbon atom to form a stable carbocation.

Answer to Problem 11.36P

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are pent1yne and pent2yne.

Explanation of Solution

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are shown as,

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 11, Problem 11.36P , additional homework tip  1

Figure 1

The terminal alkynes, pent1yne and pent2yne reacts with the reagents H2O, HgSO4 in the presence of strong acid H2SO4 to form 2pentanone as the desired product.

Conclusion

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are pent1yne and pent2yne.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are to be predicted.

Concept introduction: A terminal alkyne reacts with H2O, H2SO4 (strong acid) and HgSO4 to form a ketone. In this case, hydrogen atom and OH will get attach to the less substituted carbon atom to form a stable carbocation.

Answer to Problem 11.36P

The alkyne that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 is ethynylcyclohexane.

Explanation of Solution

The alkyne that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 is shown as,

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 11, Problem 11.36P , additional homework tip  2

Figure 2

The terminal alkyne, ethynylcyclohexane reacts with the reagents H2O, HgSO4 in the presence of strong acid H2SO4 to form 1cyclohexylethanone as the desired product.

Conclusion

The alkyne that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 is ethynylcyclohexane.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are to be predicted.

Concept introduction: A terminal alkyne reacts with H2O, H2SO4 (strong acid) and HgSO4 to form a ketone. In this case, hydrogen atom and OH will get attach to the less substituted carbon atom to form a stable carbocation.

Answer to Problem 11.36P

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are hex2yne and hex3yne.

Explanation of Solution

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are shown as,

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 11, Problem 11.36P , additional homework tip  3

Figure 3

The terminal alkynes, hex2yne and hex3yne reacts with the reagents H2O, HgSO4 in the presence of strong acid H2SO4 to form hexan3one as the desired product.

Conclusion

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are hex2yne and hex3yne.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are to be predicted.

Concept introduction: A terminal alkyne reacts with H2O, H2SO4 (strong acid) and HgSO4 to form a ketone. In this case, hydrogen atom and OH will get attach to the less substituted carbon atom to form a stable carbocation.

Answer to Problem 11.36P

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are but1yne and but2yne.

Explanation of Solution

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are shown as,

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<, Chapter 11, Problem 11.36P , additional homework tip  4

Figure 4

The terminal alkynes, but1yne and but2yne reacts with the reagents H2O, HgSO4 in the presence of strong acid H2SO4 to form butan2one as the desired product.

Conclusion

The alkynes that forms the given ketone as the only product after hydration with H2O, H2SO4 (strong acid) and HgSO4 are but1yne and but2yne.

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Chapter 11 Solutions

ORG.CHEMISTRY CONNECT ACCESS>CUSTOM<

Ch. 11 - Problem 11.11 Draw the keto tautomer of each...Ch. 11 - Prob. 11.12PCh. 11 - a Draw two different enol tautomers of...Ch. 11 - Prob. 11.14PCh. 11 - Problem 11.15 Draw the organic products formed in...Ch. 11 - Problem 11.16 What acetylide anion and alkyl...Ch. 11 - Problem. 11.17 Show how , and can be used to...Ch. 11 - Prob. 11.18PCh. 11 - Draw the products of each reaction. a. b.Ch. 11 - Prob. 11.20PCh. 11 - Problem 11.21 Use retrosynthetic analysis to show...Ch. 11 - Prob. 11.22PCh. 11 - Give the IUPAC name for each compound. a. b.Ch. 11 - Prob. 11.24PCh. 11 - 11.25 Answer the following questions about...Ch. 11 - 11.26 Give the IUPAC name for each alkyne. a. ...Ch. 11 - Prob. 11.27PCh. 11 - Which of the following pairs of compounds...Ch. 11 - Prob. 11.29PCh. 11 - 11.30 How is each compound related to A? Choose...Ch. 11 - Prob. 11.31PCh. 11 - Prob. 11.32PCh. 11 - 11.33 Draw the products formed when is treated...Ch. 11 - What reagents are needed to convert (CH3CH2)3CCCH...Ch. 11 - Prob. 11.35PCh. 11 - 11.36 What alkynes give each of the following...Ch. 11 - 11.37 What alkyne gives each compound as the only...Ch. 11 - 11.38 Draw the organic products formed in each...Ch. 11 - 11.39 Draw the structure of compounds A-E in the...Ch. 11 - Prob. 11.40PCh. 11 - Prob. 11.41PCh. 11 - 11.42 What reactions are needed to convert alcohol...Ch. 11 - Prob. 11.43PCh. 11 - Prob. 11.44PCh. 11 - 11.45 Explain the following statement. Although ...Ch. 11 - 11.46 Tautomerization in base resembles...Ch. 11 - 11.47 Draw a stepwise mechanism for each...Ch. 11 - Prob. 11.48PCh. 11 - Prob. 11.49PCh. 11 - 11.50 What acetylide anion and alkyl halide are...Ch. 11 - 11.51 Synthesize each compound from acetylene. You...Ch. 11 - 11.52 Devise a synthesis of each compound using ...Ch. 11 - Prob. 11.53PCh. 11 - Prob. 11.54PCh. 11 - 11.55 Devise a synthesis of the ketone, , from ...Ch. 11 - 11.56 Devise a synthesis of each compound using ...Ch. 11 - Prob. 11.57PCh. 11 - Prob. 11.58PCh. 11 - 11.59 N-Chlorosuccinimide (NCS) serves as a source...Ch. 11 - 11.60 Draw a stepwise mechanism for the following...Ch. 11 - 11.61 Draw a stepwise mechanism for the following...Ch. 11 - Prob. 11.62PCh. 11 - 11.63 Write a stepwise mechanism for each of the...Ch. 11 - Prob. 11.64PCh. 11 - 11.65 Explain why an optically active solution of ...
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