Please use the E/Z notation when specifying stereochemistry remembering to use parentheses and a dash. Reminder - the double bon
d takes precedence over alkyl groups when numbering the parent. (E)-5-bromo-5-ethylhept-2-ene when combined with NaOCH2CH3.
1 answer:
Answer:
(E)-5-ethylhepta-2,4-diene
Explanation:
The (E)-5-bromo-5-ethylhept-2-ene will undergo an E2 reaction. The ethoxide (⁻OCH₂CH₃) will deprotonate at the allylic position so that a conjugated diene results, which is more stable than a non-conjugated diene.
The stereochemistry in the name of the final product is indicated for only one double bond since the other has two identical groups on it.
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Explanation:
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In this case, according to the given information it turns out possible for us to realize that one mole of the given compound, Mg(ClO₄)₂, has one mole of Mg, two moles of Cl and eight moles of O; thus, we proceed as follows:
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