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Which of the following can reduce an alkene to an alkane?
Neither lithium aluminum hydride, nor sodium borohydride will reduce C–C double bonds.
H2/Raney nickel and H2/Pd can each (individually) reduce an alkene to an alkane. Since both H2/Raney nickel and H2/Pd can reduce the alkene, the answer is both of those reagents. This is a catalytic hydrogenation reaction, and H2/Raney nickel not only reduces C–C double bonds, but also carbonyl compounds.
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Identify the major organic product expected from the acid-catalyzed dehydration of 2-methyl-2-pentanol.
The initial compound is a five-carbon alkane chain with methyl and hydroxy groups on the second carbon. Dehydration involves the hydrogenation of the hydroxy group. That group then leaves, and a double bond is formed. Zaitsev's rule states that double bonds are more stable on more highly substituted carbons. The double bond forms across carbons two and three.
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If an alkane is reacted with excess in a high temperature environment, what are the products formed?
Whenever an alkane is reacted with excess oxygen in a high temperature reaction, the reaction is known as combustion. Combustion of an alkane always produces carbon dioxide gas and water vapor.
Therefore the correct answer is: and
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