An alkyl halide reacts with OH⁻ by the SN2 mechanism. If is doubled and is tripled, the rate becomes ____.
Correct answer B. 6 times the original
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Correct answer B. 6 times the original
Correct answer D. 2 times the original
Correct answer C. Tertiary > secondary > primary > methyl
Correct answer C. Polar protic, such as water
Correct answer A. Ethanol
Correct answer A. Concentrated alcoholic KOH and a high temperature
Correct answer B. The base removes a β-hydrogen as the C–X bond breaks, in a single step
Correct answer D. first order, proceeding via a carbocation intermediate
Correct answer B. But-2-ene
Correct answer B. 6
Correct answer B. BF₃
Correct answer B. its π bond is weaker than a σ bond and its electrons are exposed to electrophiles
Correct answer B. Ethene
Correct answer D. 2-Methylbut-2-ene
Correct answer B. 2-Bromopropane
Correct answer B. 32 g
Correct answer C. between a C–C single bond (154 pm) and a C=C double bond (134 pm)
Correct answer B. 6
Correct answer C. Substitution keeps the stable delocalised π system intact, whereas addition would destroy it
Correct answer C. NO₂⁺