ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
10th Edition
ISBN: 9781260028355
Author: Carey
Publisher: MCG CUSTOM
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Chapter 24, Problem 38P
Interpretation Introduction

Interpretation:

The mechanism for the given reaction is to be written.

Concept introduction:

The vicinal diols, on reaction with ketone in the presence of acidic condition, forms an acetal.

The ketone protonates and forms hemiacetal by a nucleophilic attack of hydroxyl group of vicinal diol. The hemiacetal on protonation followed by nucleophilic attack of second hydroxyl group of vicinal diol forms acetal.

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personality of each of them in terms of nucleophile vs. electrophile (some can be considered acids/bases but we are not looking at that here). Note you may have to use your growing intuition to figure out the personality of one of the molecules below but I believe in you! Rationalize it out based on what we have called strong versus weak electrophiles in past mechanisms. Consider using the memes below to help guide your understanding! A OH O B CH3 C Molecule A: [Select] Molecule B: [Select] Molecule C: [Select] Molecule D: [Select] > H D OH
4) Which oxygen atom in the structure below is most basic / nucleophilic? Please explain by discussing the electron density around each oxygen atom. Show at least three resonance structures for the compound. оого
Can you show me this problem. Turn them into lewis dot structures for me please and then answer the question because I cant seem to comprehend it/ The diagrams on the picture look too small I guess.
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