The hydration of three C5H10 alkene isomers can give 2-methylbutan-2-ol. Draw them.
10. Addition Reactions
Acid-Catalyzed Hydration
- Textbook Question
- Textbook Question
Suggest an arrow-pushing mechanism that accounts for the formation of the following products.
(a)
- Textbook Question
Predict the products you would get when the following alkenes react under the following conditions: (i) H2SO4 , H2O
(a)
- Textbook Question
Predict the product(s) that would result when the alkenes shown here are allowed to react under the following conditions: (iv) H2SO4 , H2O
(b)
- Textbook Question
Predict the product(s) that would result when the alkenes shown here are allowed to react under the following conditions: (iv) H2SO4 , H2O
(g)
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Predict the product(s) that would result when the alkenes shown here are allowed to react under the following conditions: (iv) H2SO4 , H2O
(k)
- Textbook Question
Provide a mechanism for the following reactions occurring with rearrangement.
(a)
- Textbook Question
Cyclooctene is one of the smaller rings that can form a trans alkene. Would you expect cis-cyclooctene or trans-cyclooctene to react more quickly in an acid-catalyzed hydration reaction?
- Textbook Question
Devise a synthesis for each compound, starting with methylenecyclohexane and any other reagents you need.
a. 1-methylcyclohexanol
- Textbook Question
How can the following compounds be prepared from 3,3-dimethyl-1-butene?
b. 3,3-dimethyl-2-butanol
- Textbook Question
In Chapter 8, we learned about the chemistry of terpenes and the interesting reactions they can undergo. One such reaction is the acid-catalyzed conversion of nerol to terpineol. Suggest a mechanism for this transformation
.
- Textbook Question
The acid-catalyzed dehydration we learned in this chapter is reversible, as shown below.
(a) Propose a mechanism for the formation of an alcohol from an alkene.
- Textbook Question
The acid-catalyzed dehydration we learned in this chapter is reversible, as shown below.
(c) Which side of the reaction would be favored by running the reaction at low temperatures?
- Textbook Question
Suggest a reagent to carry out each of the following conversions to an alcohol.
(b)
- Textbook Question
Predict the product(s) that would result when the following molecules are allowed to react under the following conditions: (iii) H2SO4 , H2O . If there is no reaction, write 'no reaction.'
(a)