a. C. CH CH CH CH2 CH CH3 CH OCH,CH3 CH3 CH3 CHз -CH3 b. CH -(CH2),CH3 d. (CH2)3 OCH3 CH3CH2O OCH2CH3 O. (CH2)4 b.

When cyclohexene undergoes ozonolysis, and the resulting product is treated with excess LiAlH4, following by H₂O, the product is a diol. O True O False

NAC↔X™ Ph Ph OH Acid chlorides react with Grignard reagents to yield tertiary alcohols, two equivalents of Grignard reagent are required. The first equivalent reacts in a typical nucleophilic acyl substitution reaction to give a ketone. This ketone, however, is itself reactive in the Grignard reaction. Thus, the second equivalent adds to the ketone carbonyl carbon. Subsequent protonation yields the tertiary alcohol. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Ph :0: 1. 2 eq. CH3MgBr 2. H3O+ CH3 H3C CH3 H3C-MgBr Ph O: MgBr -CH3 CH3

Please explain how the product shown is formed from the starting materials and reagents i) HHAH н H+ & ii) Mel iii) Ag₂O heat