Chapter 8 quiz #8 PDF

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1.) What is the major elimination product obtained from the following

reaction? I II III IV 2.) Which of the following is the most reactive substrate in an E2 reaction?

I II III IV 3.) Consider the following E2 reaction. What rate equation would be observed for this reaction?

rev: 07_23_2018_QC_CS-131963 Rate = k[CH3CH2CH2Br] Rate = k[CH3CH2CH2Br][KOC(CH3)3] Rate = k[CH3CH2CH2Br][KOC(CH3)3]2 Rate = k[CH3CH2CH2Br]2[KOC(CH3)3] 4.) Which of the following statements about an E1 mechanism is not true? The reaction is fastest with tertiary alkyl halides. A better leaving group makes the reaction rate increase. The reaction follows first-order kinetics. Stronger bases favor the E1 reaction.

5.) What is the major product of the following reaction?

I II III IV 6.) Which of the following represents the rate law for an E2 reaction? Rate = k[alkyl halide] Rate = k[alkyl halide][base] Rate = k[alkyl halide]2 Rate = k[base]2 7.) What is the major elimination product in the reaction of 1-bromobutane with potassium tert-butoxide in tert-butanol? cis-2-Butene 1-Butene trans-2-Butene Butanol 8.) Which of the following is most likely to react as a base rather than a nucleophile?

I II III IV

9.) What is (are) the product(s) of the following reaction?

rev: 11_09_2018_QC_CS-147618 I and II II and III I and III I, II, and III 10.) Which of the following alkyl halide reacts the fastest in an E2 reaction?

I II III IV...