Both compounds undergoes sn1 mechanism. So carbocation intermediate formed. In second compound carbocation is more stable due to resonance. So it will undergoes faster.
help please!! 16. (3) Circle the molecule that will undergo the following reaction faster. Explain your...
circle the reaction that is faster and explain your reasoning briefly indicate the mechanism operating in each case 1. (continued) кФОосмеа ме, сот кФеосме, Mes con
which of the following reactions would undergo SN2 reaction faster ? explain your choice a) CH3I + HONa ----> b) CH3I + HSNa ----> thank you
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
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
9. (1 pt.) In chapter 8 you will learn that 1-bromo-3,5-dimethvlhexane (molecule A) can undergo the substitution reaction when treated with NaCl Вг NaCl molecule A The following molecules (B through F) will undergo similar reaction with NaCl. For which of these molecules will the rate of the reaction be exactly the same as for molecule A? Circle those molecules Explain your choice by identifying the specific type of relationship between molecule A and the other molecules (B through F)...
please explain 14. Circle the molecule that is most reactive by both SN1 and Sy2 pathways Br Br Br OCH 15. Circle the major stereoisomer formed in the E2 reaction that occurs when 4-chloroheptane is treated with NaOCH2CH
For each of the following pair of reactions, CIRCLE the reaction that will occur faster (A or B) 2. NaOH NaOH 2 CH3CH2ONa EtOH CH3CH2ONa Br NaCN NaCN
3. Circle the reaction below which is faster in polar protic solvents. OH, ,0 A. CH,CH,CH,Br — CH,CH,CH,OH + Br or CH,CH,CH,SH + Br B. CH CH.CH.BESH,RSH 4. Doubling the concentration of hydroxide in the reaction in problem #3A: A: causes the reaction mechanism to change. B: halves the rate of reaction. C: has no effect on the rate of reaction. D: doubles the rate of reaction. 5. Circle the reaction below which is faster. 70% H2O A. (CH3)3C-C 30%...
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...