Chapter 9: Q13. (page 347)
Question: Draw the structure of each transition state in the two-step mechanism for the reaction.
CH3CH2OH + H2So4 → CH3CH=CH2+ H2O
Short Answer
Answer
The mechanism is shown below.
Chapter 9: Q13. (page 347)
Question: Draw the structure of each transition state in the two-step mechanism for the reaction.
CH3CH2OH + H2So4 → CH3CH=CH2+ H2O
Answer
The mechanism is shown below.
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Get started for freeQuestion: Explain the observed trend in the melting points of the following three isomeric alcohols:
Question: Epoxides are converted to allylic alcohols with non-nucleophilic bases such as lithiumdiethylamide . Draw a stepwise mechanism for the conversion of1,2-epoxycyclohexane to cyclohex-2-en-1-ol with this base. Explain why a strong bulky basemust be used in this reaction.
Question: Draw two steps to convert (CH3)3CHOH into each of the following compounds: (CH3)2N3 , and (CH3)2CHOCH2CH3.
Question: Give the IUPAC name for each compound.
a.
b.
c.
Question: Draw the products formed when each alcohol undergoes dehydration with TsOH , and label the major product when a mixture results.
a.
b.
c.
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