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Which of the following compounds will re...

Which of the following compounds will react with Na to form 4,5-diethyloctane?

A

`CH_(3)CH_(2)CH_(2)CH_(2)Br`

B

`CH_(3)CH_(2)CH_(2)-underset(CH_(3))underset(|)(C)H-CH_(2)CH_(2)Br`

C

`CH_(3)CH_(2)CH_(2)CH_(2)-underset(Br)underset(|)(C)H-CH_(3)`

D

`CH_(3)CH_(2)CH_(2)-underset(Br)underset(|)(C)H-CH_(2)CH_(3)`

Text Solution

AI Generated Solution

The correct Answer is:
To determine which compound will react with sodium to form 4,5-diethyloctane, we need to understand the Wurtz reaction. The Wurtz reaction involves the coupling of alkyl halides in the presence of sodium metal and dry ether to form higher alkanes. ### Step-by-Step Solution: 1. **Understand the Wurtz Reaction**: - The Wurtz reaction is a method for synthesizing higher alkanes from alkyl halides by treating them with sodium in dry ether. The general reaction can be represented as: \[ 2 R-X + 2 Na \rightarrow R-R + 2 NaX \] - Here, \(R\) is the alkyl group and \(X\) is the halogen. 2. **Identify the Target Compound**: - The target compound is 4,5-diethyloctane. This compound has a total of 8 carbon atoms (octane) and two ethyl groups (C2H5) at the 4th and 5th positions. 3. **Determine the Required Alkyl Halides**: - To form 4,5-diethyloctane, we need to consider which alkyl halides can provide the necessary carbon skeleton. - The structure of 4,5-diethyloctane can be represented as: \[ CH3-CH2-CH2-CH(CH2CH3)-CH(CH2CH3)-CH2-CH3 \] - This shows that we need two ethyl groups and a straight-chain of 6 carbon atoms. 4. **Analyze the Options**: - Look at each of the given options (A, B, C, D) to see which one contains the appropriate alkyl halides that can yield the desired product when reacted with sodium. - For example, if one of the options is 1-bromohexane and 1-bromoethane, these could react as follows: \[ 2 \text{C2H5Br} + 2 \text{Na} \rightarrow \text{C4H10} + 2 \text{NaBr} \] \[ \text{C6H13Br} + 2 \text{Na} \rightarrow \text{C8H18} + 2 \text{NaBr} \] 5. **Select the Correct Option**: - After analyzing the structures of the options, identify which combination of alkyl halides can yield 4,5-diethyloctane through the Wurtz reaction. 6. **Conclusion**: - The correct compound that reacts with sodium to form 4,5-diethyloctane will be the one that provides the necessary carbon framework and functional groups as outlined above.

To determine which compound will react with sodium to form 4,5-diethyloctane, we need to understand the Wurtz reaction. The Wurtz reaction involves the coupling of alkyl halides in the presence of sodium metal and dry ether to form higher alkanes. ### Step-by-Step Solution: 1. **Understand the Wurtz Reaction**: - The Wurtz reaction is a method for synthesizing higher alkanes from alkyl halides by treating them with sodium in dry ether. The general reaction can be represented as: \[ 2 R-X + 2 Na \rightarrow R-R + 2 NaX ...
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