On treatment with sodium ethnocide in ethanol, each gives 3,4-dimethy 1-3 hexane

Question

On treatment with sodium ethnocide in ethanol, each gives 3,4-dimethy 1-3 hexane as the major distorter gives the E alkenes, and the other gives the Z alkene, Which diasternrocomer gives the Z alkenes? Following are two diastaromers of 3-bromo-2,3,4-trimethey hexane, On treatment with sodium ethnocide in ethanol, each gives 2,3,4- trimethey hexane as the major distorter gives the E alkenes, and the other gives the Z alkenes. Which diasternrocomer gives the E alkenes? Following are two diastaromers of 3-bromo-2,3,4-trimethey hexane, On treatment with sodium ethnocide in ethanol, each gives 2,4,5- trimethey hexane as the major distorter gives the E alkenes, and the other gives the Z alkenes. Which diasternrocomer gives the E alkenes?

Explanation / Answer

in all the three case E2 elimination is followed therefore elimination occur by antiperiplanar geomentry.

in the case of 3,4-dimethyl-3-hexane option b will give Z isomer

in the case of 2,3,4-trimethyl-3-hexane option a will give E isomer

in the case of 3-ethyl-2,3,4-trimethyl-3-hexane option a will give E isomer

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