An alkane C 8 H 18 is obtained as the only product on subjecting a primary alkyl halide to Wurtz reaction. On monobromination this alkane yields a single isomer of a tertiary bromide. Write the structure of alkane and the tertiary bromide.

Question

An alkane C 8 H 18 is obtained as the only product on subjecting a primary alkyl halide to Wurtz reaction. On monobromination this alkane yields a single isomer of a tertiary bromide. Write the structure of alkane and the tertiary bromide., The alkane is 2,5-dimethylhexane and The tertiary bromide is 2-Bromo-2,3-dimethylhexane, The alkane is 2,5-dimethylhexane and The tertiary bromide is 2-Bromo-2,5-dimethylhexane, The alkane is 1,5-dimethylhexane and The tertiary bromide is 2-Bromo-2,5-dimethylhexane, The alkane is 1,5-dimethylhexane and The tertiary bromide is 2-Bromo-2,3-dimethylhexane

MARKS App · Accepted Answer

Correct Option is : (B) The alkane is 2,5-dimethylhexane and The tertiary bromide is 2-Bromo-2,5-dimethylhexane

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