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-Methylcyclohexene8:16 NOO ← Question 11 of 27 ||| Choose the reagent(s) that would be most likely to complete this reaction. I ■ I I I I ■ ■ ■ RCO3H > O Submit HEE | 34% I I ■ I I I I I I I ОН rIdentify the reagents needed for the given reaction. -c-CH3 || Ĉ-CH3 || ċ-CH2B1 Select one: HBr О НBr O Br2, H20 O Br2, hv O Br2, OH
- Which of the following reagents would you use to prepare Chlorocyclopentane from cyclopentene? OC2 / H20 NBS / H20, DMSO OCh/ CH,Cl2 HCIWhich carbocation is least stable and which is most stable? Which carbocation can't be rearranged into a tertiary carbocation?K 11:00 bartle 0 H₂CCO I 29 O IV, I, II, III O III, II, I, IV O III, I, IV, II More IV, III, I, II Bibimbap Chanyeol Active Now e H₂CO II Arrange the nucleophiles in order of increasing reactivity (least first). = d Br 4 III N d H₂O IV اس اس }[{ 96 Edit
- 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ⓇPredict each product for the following multistep reaction. If ortho/para products are both formed, use the para product in the next reaction. HNO3 A Cl2 Zn B NANO2 C CUCN H20 E F H2SO4 HCI HCI OH9-53 Identify the reagents a through d in the following scheme: H OH H. CH30 OCH3 Br Br