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Predict the product(s) and provide a mechanism:
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- Which intermediates are formed during the mechanism of the below reaction? Select all that apply. NaOH CH3 CH3 口 OH CH3 CH CH3 CH3 OH 2.Name this molecule. CH; CH, | CH,- CH, CH, CH, — С — сH,- сн — сн, — CH, | CH3 CH2compound name CH; – CH,– CH, - CH3- CH, — CH, — С — CH, — CH,– CH, - | CH,– CH3 CH,– CH, – CH3 CH, — CH— С — СН, — CН, — сH, - - - CH; - CH, — СH CH; - CH3 - CH - CH,- CH3 CH, CH,
- In each of these reactions, the organic starting material is achiral. The structural formula of the product is given. For each reaction, determine the following. (1) How many stereoisomers are possible for the product? (2) Which of the possible stereoisomers is/are formed in the reaction shown? (3) Will the product be optically active or optically inactive? CH3 CH3 (a) + HBr Br Br (b) / + Br2 CI, Br Br (c) + Br2 CCI, Br (d) + HCI (e) + Cl, in H,O CIWrite the systematic name of each organic molecule: OH | structure CH3 -CH–CH2–CH2–CH3 HỌ—CH2−CH2 —CH,—OH HO—CH,—CH2−CH2 —CH3 name 0 0H2 C. CH2 H,C + HCl C-CH H, OH