circle the reaction that is faster and explain your reasoning briefly indicate the mechanism operating in each case
circle the reaction that is faster and explain your reasoning briefly indicate the mechanism operating in...
Circle the reaction that is faster for each given pair of reactions and concisely explain your reasoning, being certain to clearly indicate the type of mechanism operating in each case. 1-Buok BA t-BuOH -Buok -BuOH isopropanol heat isopropanol heat көосмез Мез СОН көocМез Мез Сон
Due Wednesday 11/20/19 Before 1:00 p.m. Signature Circle the reaction that is faster for each given pair of reactions and concisely explain your reasoning, being certain to clearly indicate the type of mechanism operating in cach case. 1-Buok 1-BUOH t-BudPk 2Brine t-BUOH isopropanol heat isopropanol heat
indicate which reaction will occur faster. explain your reasoning. reaction of 1 chlorobutane with sodium iodide or sodium p toluenesulfonate in aqueous ethanol. Indicate which reaction will occur faster. Explain your reasoning. Select the single best answer Reaction of 1-chlorobutane with sodium iodide or sodium p-toluenesulfonate in aqueous ethanol Sodium iodide will react faster because the leaving group encounters less sterle hindrance. Sodium iodide will react faster because the intermediate is more stabilized in the solvent. Sodium p-toluenesulfonate will react...
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...
help please!! 16. (3) Circle the molecule that will undergo the following reaction faster. Explain your reasoning. Br Br H2O or
5. Circle the molecule that matches the best description for each set of reagents. Briefly explain your reasoning in the box provided. (a) Faster in an S12 reaction: н, сун,слуғ (b) Faster in an E1 reaction: (c) Better nucleophile: CH, H,C^NH HọcCH, Học-NH, (d) Better base: no homo
For each pair of reactions given below indicate which is faster and explain your reasoning: HO (CH3),CHBT (CH),CH-OH но (CH3),CBr - (CH),C-OH acetone CH,CH,0 + CH.CH,Br CH,CH,OCH,CH, + Br acetone CH,CH,S + CH,CH_Br > CH CH SCH,CH2 + Br (CH3),COH + KBr -- (CH), CBr + KOH (CH3),COH + HB (CH) CB + H2O СН.ОН (CH3),CHBr (CH3),CH-OCH CHOH (CH3),CBr (CH3),C-OCH, "SH + Br Br + HS - "SH + Bri Br + HS
4. For the following pairs of reactions, clearly circle the reaction you believe would occur foster Briefly, using chemical principals, describe in the space below why you made your decision Also, indicate in the box which mechanism (S1, S2, E1, E2) would be the likely mechanism of the reaction you circled. (5 pts each) PHOSO CF, NaCN DMF Ph CN oso,CF, DMF Mechanism of circled reaction NaOme NaOme (E)-3-methyl-2-pentene - (Z)-3-methyl-2-pentene MeOH, A MeOH, A Mechanism of circled reaction KBr...
please explain the work ch of the following pairs of organic molecules or lons, circle the one that is the better nucleophile, and briefly explain your choice. for each of the Holon von Hello "es-CN vs. oo-on H₂C NH₂ vs. Ha Ha H₃CNH2 4. For each of the following pairs of organic molecules, circle the one that would react with a given nucleophile at a faster rate in the Su2 reaction, and briefly explain your choice. amor