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Chem 233 Exam III (A) October 28, 2019 Page 7 14. Which of the following would...
Q1) Which compound will undergo SN1 reaction fastest? CI Cl Q2) What is true about SN1 reaction of alkyl halides? a) Reaction favored by non-polar solvents. b) Reaction rate depends on concentration of alkyl halide c) SN1 proceeds in one step thru transition state d) Reaction rate depends on concentration of nucleophile
16. Which of the following is correct regarding Sy2 reactions of alkyl halides? A. Secondary halides react faster than primary halides. B. Rate of reaction depends on the concentrations of the alkyl halide only. C. Favored in polar aprotic solvents D. Results in a racemic mixture
20) Which of the following statements is true about SN1 reactions of alkyl halides? A) The reactions are favored by polar solvents. B) The reaction occurs via a one-step back-side attack. C) Complete inversion of configuration occurs. D) Reaction rates depend only on the concentration of the nucleophile. E) The reactions are favored by nonpolar solvents.
need help with these practice problems please :) if can help with
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A. Predict how reaction conditions (substrate, nucleophile, leaving group, solvent) effect the rate of Swi and S2 reactions. Circle the faster substitution reaction among the following pairs. If the rate is not affected, circle both OH OH in acetone ta NaBr DMSO in H2O NaBr CH, OH V CI Br- na ro ChOH CHCI Bra CHCI ? © CN acetone CI- in H20 in...
17. Which of the following statements is true? A. An Sw1 reaction always proceeds faster than an S2 reaction. B. An Sw2 reaction is not stereospecific C. Good alkyl halide substrates for an E1 reaction are also good for an E2 reaction. D. Increasing the alkyl halide concentration enhances the reaction rate of an Sw1 reaction but not that of an E2 reaction. 18. For the following reaction, what happens to the reaction rate if the concentration of NaN, is...
6. Which correctly depicts the displacement of bromide by hydroxide? a) HỐ Br CH2 6) HỘ CH₂ Car c) Ho Br CH₂ d) HÓ CH - Br 7. Which is true about Sn2 reactions? A) Polar aprotic solvents are used in the reaction B) 1° halides react slower than 30 halides C) Rate of reaction depends on both nucleophile and halide D) A and C E) A, B and C
28) The reaction of tert-butyl bromide, (CH,)CBr, with ethanol affords the substitution product tert-butyl ethyl ether, (CH)1COCH CH, in acidic conditions. What would happen to the rate of the reaction if the concentration of ethanol was doubled? A) The rate remains the same. B) The rate decreases by a factor of 2 C) The rate increases by a factor of 2. D) The rate increases by a factor of 4. Circle the following alkyl halide that will undergo the fastest...
Which statement or set of conditions listed below is not consistent with an Syl reaction pathway? O a. Neutral nucleophile work just fine. b. The leaving group is typically the conjugate base of a strong acid. O c. The rate is not dependent upon the concentration of the nucleophile. d. The temperature is relatively "cooler" to reduce competing elimination products. e. The solvent is polar and aprotic. Of. The substrate has a leaving group that is typically on a 30,...
5) (marks = 3) Please answer the following as TRUE or FALSE in the space provided to the left of each statement (0.5 marks each). True/False All tertiary alkyl halides only participate in SN 1 reactions. CH30 is a better nucleophile for an SN2 reaction than CH3S when in methanol. The relative stability of carbanions is as follows: (most stable) 1° >2 > 30 (least stable) Unlike other alkyl halides (CI, Br, 1), alkyl fluorides do not participate in substitution...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...