Please answer all. thanks QUESTION 5 HO Reaction C Reaction D Consider the structural changes that...
C. Indicate which is the late-detemning step. d. Is it the same mechanism as in question 1? Why or why not? 3. Explain why El and Sx1 mechanisms follow first order reaction kinetics, whereas E2 and SN2 mechanisms follow second order reaction kinetics. 4. Which is the better nucleophile in a protic solvent: chloride ion or bromide ion? Try to explain this in terms of the nature of the chloride ion and the bromide ion. 5. For the synthesis of...
Consider the reaction below to answer the following question(s). Ci H2O A CH3 CH3 Compound B is the: O E1 product E2 product SN1 product O SN2 product
please answer both questions c omo se torn. c 1. BBr, heat 2. H2O . an. som • сн,в • Вон) Hypo НРО 165 . O . How a = Proton transfer b - Lewis acid/base c = Electrophilic addition d-E1 Elimination e E2 Elimination 1-Syl Nucleophilic substitution 8 = SN2 Nucleophilic substitution The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a-g...
please give correct answer to these 5 questions with explanations, thankyou Select the structural features that nucleophiles typically contain What is the best reagent to use for the following substitution reaction? Select one or more: Negative charges Lone pairs Unpaired electrons Double bonds Positive charges Select one: MgBr Which of the following molecules are most likely to react as electrophiles? ob. NaOH COOH Select one or more w occo oor on ll“ fot Complete the following sentence to produce a...
PLEASE ANSWER ALL QUESTIONS Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
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...
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!! Name: O Determine wither a reaction proceeds via SN2, SN1, E2, and/or E1/ Predict the productís) of substitution and elimination reactions. Draw the major products), reagent(s), or starting material(s) ¡n order to complete each transformation. Indicate any stereochemistry when appropriate. If there is no reaction, write "NO RXN AND explain why no reaction occurs 1. Br NaCCMe Br b. он NaOE Me DBU d. MeOH e. CI NaSEt Chapter 8-3
Question 17 For the following reaction, which of the following is the mechanism? HBr OH A. SN1 B. SN2 C. E1 D. E2 Question 18 What is the product of the following reaction. som trosos molt sisada gniotetor H2O GA I. AG A) I B) II C) III al D) I+II istuiwell todo E) I+III HO Question 19 What reaction mechanism is most likely for substitution on the following compound? 2 Dub T o wable oil A. SN1 B. SN2...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23 Dehydration Which reagent(s) are required to perform a dehydration reaction? o a. HCI С. NaH o d. H2SO4 e. NaOH f, H2SO4, heat g. NaOH, heat QUESTION 21 Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply iv) a. C. eNone of the above. The reaction goes by an E2 mechanism and no carbocations are formed. QUESTION 22...
1. (18 points; 3 points each] Multiple Choice: Circle the best answer i. Consider the following reaction: Xooot THF, A If there are no other changes, what is the effect of doubling the concentration of the starting alcohol on the rate of this reaction? a. No change b. Doubles the rate C. Triples the rate d. Quadruples the rate ii. Which nitrogen compound below would react fastest as a nucleophile in an 5, 2 reaction? NH NH N d. "NH2...