Organic Chemistry (8th Edition)
Organic Chemistry (8th Edition)
8th Edition
ISBN: 9780134042282
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 23.2, Problem 5P

Instead of adding to the 4a position and protonating N-5, the thiolate ion could have added to the 10a position and protonated N-l. (The numbering system is on page 1071.) Why is addition to the 4a position favored? (Hint: Which nitrogen is a stronger base?)

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7. For compound A in acid, it is the hydroxyl that is protonated to a greater extent than the carbonyl oxygen. However, for compound B in acid, it is the carbonyl oxygen that is protonated to a greater extent than the hydroxyl oxygen. Explain this difference. H2SO4 ОН ОН2 ОН H2SO4 ОН ОН
Explain why the C – Ha bond is much more acidic than the C – Hb bond in pentan-2-one.
Predict the position of the equilibrium for the reaction and provide a brief explanation. (The acidic protons are shown in red.) to to OH CH3- CH3-OH A D Forward direction is favored because C is not well solvated, making Ca stronger base than B. Forward direction is favored because C is not well solvated, making Ca weaker base than B. Reverse direction is favored because C is not well solvated, making Ca weaker base than B. Reverse direction is favored because C is not well solvated, making Ca stronger base than B.

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Organic Chemistry (8th Edition)

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