Chapter 11: Q 11-11-42 E-b (page 350)
Which reactant in each of the following pairs is more nucleophilic? Explain.
b) H2O or CH3CO2-
Short Answer
CH3CO2-
Chapter 11: Q 11-11-42 E-b (page 350)
Which reactant in each of the following pairs is more nucleophilic? Explain.
b) H2O or CH3CO2-
CH3CO2-
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Get started for freeHow might you prepare each of the following molecules using a nucleophilic substitution reaction at some step?
Tell whether each of the following reactions is likely to be SN1, SN2, E1, E1cB or E2:
b)
SN2 reactions take place with inversion of configuration, andSN1 reactions take place with racemization. The following substitution reaction, however, occurs with complete retention of configuration. Propose a mechanism.
.
When primary alcohol is treated with p-toluenesulfonyl chloride at room temperature in the presence of an organic base such as pyridine, a tosylate is formed. When the same reaction is carried out at a higher temperature, an alkyl chloride is often formed. Explain.
Rank the following substances in order of their expected reactivity:
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