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hi please answer all parts , this is mu last question thank you! wilk rate ! 26. cengage said the isomer names were incorrect, please

hi please answer all parts , this is mu last question thank you! wilk rate !
26.
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cengage said the isomer names were incorrect, please check.
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Propose a structurat formuld for this compound (a) How many stercoisomers are possible for 1-methyl-1,2-cyclohexanediol? (b) Name the stereoisomers formed by oxidation of 1-methylcyclohexene with osmium tetrovide. If there is only one stereoisomer formed. leave the kamnnt wasage blank, Isomer 1: Isomer #2 : (c) Is the product formed in step (b) optically active? -ing an aikene with either hydroboration-oxidation or oxymercuration-reductidn. - You do not have to consider stereochemistry. - Indicate the method of preparation by drawing either BH3 (for hydroboration-oxidation), or Hgg (for oxymerouraticn-reduction), in i sesate siktaker - If there is more than one alkene that can be used for a gliven method, draw all of them: - If either hydroboration-oxidation or oxymercuration-reduction can be used, just give the structures for one method. - Separate structures with + signs from the drop-down menu

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