The reaction of t-butyl chloride and sodium ethoxide gives mainly

t-butyl ethyl ether

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2, 2-Dimethyl butane

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2-methylprop-1-ene

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Isopropyl-n-propyl ether

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Solution

The correct option is C 2-methylprop-1-ene
The nucleophile $O C_{2} H_{5}$ cannot attack at the carbon of bond due to steric hindrance.
Hence, elimination reaction occurs.

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When ethyl chloride is added to Sodium tert-butoxide, ethyl tert-butyl ether is obtained as the major product (shown below):

When the concentration of ethyl chloride is doubled, the reaction rate:

Q. Assertion :

t e r t

-Butyl bromide

({M e}_{3} C - B r)

and sodium ethoxide

(N a O E t)

will react to form only ether Reason: Ethers are prepared from sodium alkoxide and alkyl halide

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When the concentration of ethyl chloride is doubled, the reaction rate:

Q. Assertion :

t

-Butyl romide on reaction with sodium metal in dry ether gives

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t

-Alkyl halides readily undergo Wurtz reaction.

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The reaction of t-butyl chloride and sodium ethoxide gives mainly

The correct option is C 2-methylprop-1-eneThe nucleophile OC2H5 cannot attack at the carbon of bond due to steric hindrance. Hence, elimination reaction occurs.

The correct option is C 2-methylprop-1-ene
The nucleophile $O C_{2} H_{5}$ cannot attack at the carbon of bond due to steric hindrance.
Hence, elimination reaction occurs.