(a) Interpretation: The reaction conditions that are needed to convert ( R ) -2-ethyl-2-methyloxirane to ( R ) -2-methylbutane-1, 2-diol are to be predicted. Concept introduction: The opening of an epoxide /oxirane ring is regioselective either it takes place with a strong nucleophile ( :Nu − ) or an acid ( HZ ) . The mechanism of the reaction with :Nu − is S N 2 , and the mechanism of the reaction with HZ is in between S N 2 and S N 1 .
(a) Interpretation: The reaction conditions that are needed to convert ( R ) -2-ethyl-2-methyloxirane to ( R ) -2-methylbutane-1, 2-diol are to be predicted. Concept introduction: The opening of an epoxide /oxirane ring is regioselective either it takes place with a strong nucleophile ( :Nu − ) or an acid ( HZ ) . The mechanism of the reaction with :Nu − is S N 2 , and the mechanism of the reaction with HZ is in between S N 2 and S N 1 .
Solution Summary: The author explains that the reaction conditions that are needed to convert (R)2-methylbutane-1, 2-diol are to be predicted.
Definition Definition Special class of cyclic ethers (R-O-R') with a three-atom ring. Epoxides are an important functional group in organic chemistry as they generate reactive centers due to their unusual high reactivity. This high reactivity make epoxides toxic and mutagenic.
Chapter 9, Problem 9.69P
Interpretation Introduction
(a)
Interpretation: The reaction conditions that are needed to convert (R)-2-ethyl-2-methyloxirane to (R)-2-methylbutane-1, 2-diol are to be predicted.
Concept introduction: The opening of an epoxide/oxirane ring is regioselective either it takes place with a strong nucleophile (:Nu−) or an acid (HZ). The mechanism of the reaction with :Nu− is SN2, and the mechanism of the reaction with HZ is in between SN2andSN1.
Interpretation Introduction
(b)
Interpretation: The reaction conditions that are needed to convert (R)-2-ethyl-2-methyloxirane to (S)-2-methylbutane-1, 2-diol are to be predicted.
Concept introduction: The opening of an epoxide/oxirane ring is regioselective either it takes place with a strong nucleophile (:Nu−) or an acid (HZ). The mechanism of the reaction with :Nu− is SN2, and the mechanism of the reaction with HZ is in between SN2andSN1.
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Quiz List - RCC430M_RU05 X
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Draw a resonance structure of pyrrole that has the same
number of pi bonds as the original structure. Include all lone
pairs in your structure.
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