Answer:
The compound a is 1-methyl cyclohexene (see attachment for structure).
Explanation:
The reaction of 1-Bromo-1-methylcyclohexane with sodium methoxide is a <u>second-order reaction</u> since the <u>methoxide ion is a strong base</u> and also a strong nucleophile. This ion attacks the alkyl halide faster than the alkyl halide can ionize to produce a first-order reaction. However, we can not see the product of nucleophilic substitution. The SN₂ mechanism is blocked due to the <u>impediment of the 1-Bromo-1-methylcyclohexane</u>. The main product, according to the Zaitsev rule, is the 1-methyl cyclohexene, thus forming a <u>double bond</u>.
Then, this cyclohexene is hydrogenated to form the cyclohexane.
The arrangement of electron pairs around CH4 and NH3, According to the VSEPR model is the same, because in each case there are the same number of electron pairs around the central atom. So the NH3 and CH4 arrangement of electron pairs is the same because in each case there are the same number of electron pairs around the central atom.
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