1,3-Cyclopentadiene has to be used quickly after it is made, or stored cold. Which reaction below is the reason it has to be used so quickly? 10.1-0 A B C + H₂O HO D + H2O S OH O O C O D A B
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- 7-55 trans-1-Bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcyclohexene on treatment with KOH. What does this result tell you about the stereochemistry of E2 reactions? CH3 .CH3 кон Br H trans-1-Bromo-2-methylcyclohexane 3-MethylcyclohexeneWhat are the reagents A and B in the scheme below? Br CH3 в CH,CH,CH,C-CH, A HgC CHy H;C CHElimination reactions of cis- and trans-1-bromo-2-methylcyclohexanes with Eto in ETOH could potentially give the two products, 1-methylcyclohexene (1) or 3-methylcyclohexene (2). Which answer (a-d) indicates the major products for each reaction? Br „Br EtO Eto "CH3 ELOH `CH3 *CH ELOH "CH3 cis trans Select one: a. 2 from the cis and 1 from the trans substrate b. 2 both from the cis and trans substrates c. 1 both from the cis and trans substrates d. 1 from the cis and 2 from the trans substrate
- 7Which alkene choices and reaction conditions created this product?Draw a structural formula for the major product of the reaction shown. Cl₂ H₂O Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. If the reaction produces a racemic mixture, just draw one stereoisomer. 8 Sn [F ChemDoodleⓇ
- Give detailed Solution with explanation neededTreatment of alkenes A and B with HBr gives the same alkyl halide C. Draw a mechanism for each reaction, including all reasonable resonance structures for any intermediate. Br -CHCH2CH, HBr HBr -CH=CHCH, -CH2CH=CH2 A B.alkyl halide V Br OH Me when treated with NaOH, He E2 elimination only gave a single alkere isomer rotate the newman structure that was drawn down the bond shown by the arrow to show the confirmation of the E2 result, then draw the sole alkene isomer and label it cis or trans isomer