Which of the following alkyl halides gives the slowest SN2 reaction? O 1-chloro ethane O 1-chloro-2-methyl propane 2-chloro-2-methyl butane 1-chloro-2-methyl butane
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- True or false? 2-bromo-2-methylpropane undergoes SN1 rather than SN2 because the nucleophile experiences steric hindrance, and a stable carbocation can be formed. When hydroxide ion reacts with 1-chloropropane the main product is 1-propanol.Which of these nucleophiles would be the best for converting a tertiary alkyl halide into an alcohol? CH3O- CH3OH H3O+ OH- H2O9. Which of the following nucleophiles can undergo a substitution reaction with an alcohol under strongly acidic conditions? NH₂ - A B Br C D MgBr
- Which of the following compounds undergoes the most rapid nucleophilic substitution with hydroxide ion? Br Br Br CH3 Br CH3 NO2 CH3 4 3 2 1 2 3 4Which of the following alkyl halides undergoes the fastest SN2 reaction? 1-iodohexane 1-fluorohexane 1-bromohexane 01-chlorohexane Moving to another question will save this response. O OWhat is the major organic product obtained from the following sequence of reactions? 2 mol Br (Z)-6-methyl-2-heptene 2 mol Li Et₂0 (E)-4-methyl-2-pentene 2-methylheptane 3-methylheptane 1 mol Cul Et₂0 1 mol Br
- Which of the following labelled hydrogens will be the most susceptible for base-abstraction in an elimination reaction mechanism? H₂ H₂ 0000 He Ha H₂ H₂ H₂ Hd Br t-BuOH A 4Why do cis-1-bromo-2-ethylcyclohexane and trans-1-bromo-2-ethylcyclohexane form different major products when they undergo an E2 reaction?Arrange the following alky halides in order of decreasing reactivity in an SN1 reaction: 2-bromopentane, 2-chloropentane, 1-chloropentane, 3-bromo-3-methylpentane
- The reaction of 1-bromobutane with which of the following nucleophiles is a carbon chain-lengthening reaction? sodium acetylide (NaC=CH) sodium hydroxide (NaOH) O ammonia (NH3) potassium iodide (KI)Which best describes the first step of the mechanism of the reaction below? + CH₂MgBr H3C 1) ether 2) H3O+ → CH3 CH3MgBr acts as an nucleophile and attacks the carbonyl carbon. The carbonyl carbon acts as an nucleophile and attacks CH3MgBr. The methyl group on acetone leaves forming a carbonyl carbocation. O CH3MgBr acts as an electrophile and attacks the carbonyl oxygen.Answer the question below the reaction. OH tom ta + H₂O In the second step of the reaction mechanism, which of the following is formed? H3C H3C H3C H3C + Excess NH4C1 CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 H₂SO4