Chapter 9: Q2. (page 335)
Question: Give the IUPAC name for each compound.
a.
b.
c.
Short Answer
Answer
a.3,3-dimethyl-1-pentanol
b.cis-2-methylcyclohexanol
c. 5-ethyl-6-methyl-3-nonanol
Chapter 9: Q2. (page 335)
Question: Give the IUPAC name for each compound.
a.
b.
c.
Answer
a.3,3-dimethyl-1-pentanol
b.cis-2-methylcyclohexanol
c. 5-ethyl-6-methyl-3-nonanol
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Get started for freeQuestion: What alkyl halides are formed when each ether is treated with HBr?
a.
b.
c.
Question: a) What is the major alkene formed when A is dehydrated with ? (b) What is the major alkene formed when A is treated with and pyridine? Explain why the major product is different in these reactions.
Question: Draw the organic product of each reaction.
a.
b.
c.
d.
Question: The cis and trans isomers of 2,3-dimethyloxirane both react with –OH to give butane-2,3-diol. One stereoisomer gives a single achiral product, and one gives two chiral enantiomers. Which epoxide gives one product and which gives two?
Question: An allylic alcohol contains an OH group on a carbon atom adjacent to a double bond. The treatment of allylic alcohol A with HCl forms a mixture of two allylic chlorides, B and C. Draw a stepwise mechanism that illustrates how both products are formed.
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