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i. Z-2,3-Dideuteroeo-but-2-ene overset("...

i. Z-2,3-Dideuteroeo-but-2-ene `overset("Hydroboration")underset("bromination")rarr`
ii.E-2,3-Dideutereo-but -2-ene `overset("Hydroboration")underset("bromination")rarr`
iii. 1,2-Dideutereo cyclohexene `overset("Hydroboration")underset("bromination")rarr`

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To solve the question, we will analyze the reactions step by step for each compound mentioned. The reactions involve hydroboration followed by bromination. ### i. Z-2,3-Dideutero-but-2-ene 1. **Structure Identification**: The starting compound is Z-2,3-Dideutero-but-2-ene. This means we have a double bond between the second and third carbon atoms, and both of these carbons have a deuterium (D) substituent. The structure can be represented as: ``` D D \ / ...
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