Compounds X and Y are both C6H13Cl compounds formed in the radical chlorination of 3- methylpentane. Both X and Y underg

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Compounds X And Y Are Both C6h13cl Compounds Formed In The Radical Chlorination Of 3 Methylpentane Both X And Y Underg 1 (46.97 KiB) Viewed 11 times

Compounds X and Y are both C6H13Cl compounds formed in the radical chlorination of 3- methylpentane. Both X and Y undergo base-promoted E2 elimination to give a mixture of alkenes. In water X and Y each react to form a mixture of substitution and elimination products; however, X reacts much faster than does Y. What is the structure of Y? Do not use stereobonds in your answer. • In cases where there is more than one possible structure for each molecule, just give one for each. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. / [] nکر