1. Which of the following takes place faster by an S2 reaction! 2. Rank from strongest...
For the following reaction, identify the nucleophile, electrophile, and leaving group. 0 + A Br AB Nucleophile (Select] Electrophile (Select] Leaving Group (Select] Consider the following molecules: Br Ver - H Which will react the fastest in an SN2 reaction? [Select] Which will react the fastest in an E2 reaction? (Select]
2. Which SN2 reaction in each set will take place faster? Give the product for each reaction and give a short explanation of why one takes place faster. a + HO Br + HO b) CH,Br HO CH3BT + H2O c) CHCI + HO CH31 + HO- d) CH2Br + H2O CH3Br + NH3 e) CH2Br DMSO CH3Br + HO CH3CH2OH Page 1
CHEM 2123/Pre-Lab Study Questions /Exp. #6 Reactivities of Alkyl Halides in Nucleophilic Subs. Reactions Amonda salas Name 1. Classify the following substrates as 1°, 2, 3, aryl, allylic, or benzy lic: CH OCH CHB сна 2. Identify the substrate, nucleophile/base, and the leaving group in the following reactions and indicate the type of reaction (i.e. SN1, SN2, EI, E2) taking place: Br Nal Accionc H.с н.с Нас, CH,OH HEAT сH,он CH-Br Н-о CH CHs CH,CH-ONa HEAT Нс CH3 3. Rank...
please answer all of the following questions. 1. [03 pts. For the following reaction, label the nucleophile, electrophile, and leaving group. nucleophile" Lexleasing group 2. [03 pts. Rank the following substrates from most to least reactive in an S2 reaction. 3. [02 pts.) Which of the following is the reaction diagram for endothermic Sn2 reaction? Xo 4. [03 pts.] Draw the major product for the following Sn2 reaction. NaCN 5. [02 pts.) Which reaction in the following pair takes place...
1. What is the nucleophile in the following S2 reaction and what is the leaving group? + NaCN 2. What are products of the following sequences of elementary steps? 1. Proton transfer involving NaOH 2. Nucleophile elimination 3. Nucleophilic addition of CH Mgr 4. Sy2 involving CH Br 1. Electrophilic addition of Ci 2. Electrophile elimination of H3C (b) (c) 1. E2 involving NaOCH, 2. Electrophilic addition involving H™ 3. Coordination involving H2O 4. Proton transfer involving H 0 осн,...
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,...
What is the major Organic product from the following sequence of reactions? 1) NaNH2 2) Br W u on ou oh oh oh NH (a) (d) (e ) a. a b.b d. d e. e f. f Arrange the following species in order of increasing nucleophile strength in an SN 2 reaction. h:1-, CH3NH2, CH301- O a. (Weakest nucleophile) CH3NH2 < CH301- <H:1- (Strongest Nucleophile) O b. (Weakest nucleophile) CH3NH2 <H:1- < CH301- (Strongest Nucleophile) OC (Weakest nucleophile) CH301- <h:1-...
1. What is the nucleophile in the following S2 reaction and what is the leaving group Br + NaCN 2. What are products of the following sequences of elementary steps? ci 1. Proton transfer involving NaOH 2. Nucleophile elimination 3. Nucleophilic addition of CH,MgBr 4. Sy2 involving CH Br (c) 1. Electrophilic addition of C 2. Electrophile elimination of HC (b) 1. E2 involving NaOCH, 2. Electrophilic addition involving H 3. Coordination involving H20 4. Proton transfer involving H2O OH...
answer all 1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...
Which of the following reactions will undergo an E1 reaction faster? Question 2 Not yet answered Points out of 1.0 P Flag question (a) C (b) (c) (d) Select one: O a. (a) 1-bromopentane O b. (b) E-1-bromo-1-pentene c. (C) 3-methyl-3-bromopentane O d. (d) 3-methyl-3-bromo-1-pentene O e. The two fastest of these will have exactly the same rate constant. True or false: When both an SN2 and an E2 reaction are possible, increasing the temperature of the reaction will speed...