Which, if either, of the two cyclohexyl bromides below would react faster with strong base? A Br CHỊCH,ONG or B Br ۵ A OB O they would have the same reactivity O neither of these bromides cold react under these conditions
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- Which compound reacts fastest in an E1 rxn. The correct answer is C but explain why it is correct and why the other options are incorrect. thanks :)H. H ÔMe Ph;P LIAIH4 compound a compound b HO. Bombykol C16H300 The above reaction scheme presents one possible synthesis of the compound. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound b. Consider E/Z stereochemistry of alkenes. Do not show stereochemistry in other cases.Rank the four arometic rings below by reactivity (least reactive to most reactive) when mixed with the following benzenediazonium ion.
- Complete the following reaction scheme. Give all product(s) and indicate major or minor and any relevant stereochemistry (d) dil HCl (e) ОН Conc H2SO4 heat (f) HBrDoes cis- or trans-1-bromo-4-tert-butylcylohexane react faster in an E2reaction?Which one of the following reagents would be the correct hydride source to accomplish the chemical transformation as shown? ? H2, Raney Ni o LIAIH4 O LIAI[OC(CH3)3]3H O NABH4 O [[CH3)2CHCH2]2A|H
- Predict the the regiochemical outcome (major product) for each of the following reaction, and explain why. (Draw complete resonance structures.) CN ÇO,Et EtO MeoWhich of the following compounds reacts with HBr more rapidly?V. @Given the following mechanism fer me Y OCHS NaOH reaction show the detailed conversion of A to B •OCN3 CH3OH. OH (A) (B) c Ⓒ using the same detailed mechanism instead of cyclonexare ring as shown in product. B, propose and fer a product wil a cyclopentane ning instead of a cyclohexane viny. Ⓒ Exploumpand I with why campand (B) is preferred over the campanay campand with a cyclopentake ring..