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Chapter 9: Q23. (page 358)

Question: Draw two steps to convert (CH3)3CHOH into each of the following compounds: (CH3)2N3 , and (CH3)2CHOCH2CH3.

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Answer

Step by step solution

01

Step-by-Step Solution Step 1: Conversion of alcohol to alkyl halide

There are different reagents used to convert alcohol to alkyl halide. The reagents that are used for conversion are based on the classification of the alcohol.

02

Formation of the product

The two steps for the conversion of CH32CHOHtoCH32CHN3 are shown below.

Formation of 2-azidopropane

The two steps for the conversion of CH32CHOHtoCH32CHN3 are shown below.

Formation of 2-ethoxypropane

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Most popular questions from this chapter

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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Question: Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3I ; (b) TsCl and pyridine, followed by NaOCH3 ; (c) PBr3, followed by NaOCH3. Which two routes produce identical products?

Question: When each halohydrin is treated with NaH a product of molecular formulaC4H8Ois formed. Draw the structure of the product and indicate its stereochemistry.

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