Which attacking species shown below would be the best choice to enforce an E2 pathway over...
Which attacking species shown below would be the best choice to enforce an E2 pathway over an SN2 pathway for the reaction below? Attacking Species? BI CH; H -¢-o CH,MgB HC-0-0 CH; (a) H (b) (c) NH OH (d) SH (1) e Which solvent(s) listed below would be satisfactory in Sn2 reactions? HzC CH DMSO CH3CH,OH o HzC. Н.С DMF I II III a. I only b. II only c. III only d. I and II e. I and III...
Question 10 What reagents is the best choice for achieving the following chemical transformation? O 0 ?? CH CC1; a. Cl2, NaOH b. PC13 Ос. HCI, А d. NaCl, H20 e. Cl2, AcOH Of. Cl2 Question 11 Which attacking species shown below would be the best choice to enforce an E2 pathway over an Sp2 pathway for the reaction below? Attacking Species? Br H CH CH3MBI HCO HC O H (b) CH NH OH (a) SH ( a. a Сь....
Question 9 Which is the attacking species that would favor E2 over SN2? Loh A B
1. Which of the following species acts as the electrophile in the reaction shown below? Demo b. HyC-ce-CH, HC-C-CH, HC-G=CH₂ AICI HyC-CH-CH 2. Which of the labeled sites (a-d) on the compound shown below will be the preferred site of chlorination upon reaction of the compound with Cla with FeCl ? 3. Which of the following sets of reagents is the best choice to complete the reaction shown below? of — OY a. NH NHz with KOH and heatb. Hz...
What is the best choice for the preparation of tert-butylmethyl ether shown below? CH; HC-º-0-CH; CH CH; a) Hzc-c-OH H.SO + CH3OH CH CH b) H;C-C-o Na CH31 - CH; CH, c) H3C-Ć-1 CH30 Na CH - CH d) H;C-C-OH CH; H 1) CHzMgBr, ether 2) H30* (e) Br--C H CH; d-o CH;
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,...
For letters h & i : For each of the following reactions, predict the major mechanistic pathway (SN1/SN2/E1/E2) and the major organic products 1. (cont.) (h) НСОН CHB -CHBr HCOH - (0) CH,CH,CH,CH,Br- NH 2. For each of the following indicate which reaction will occur faster. Explain your reasoning. (No credit will be given for guesses) (a) The reaction of (CH),CBr with 0.001M aqueous NaOH or 0.10M aqueous NaOH (b) The reaction of 2-bromobutane with NaOH in DMSO or NaSH...
What is the major organic profucy expected from the following reaction? (more questions below if you can help it would be much appreciated!!) What is the major Organic product expected from the following reaction? OH оно ci CH:CH OH OH OCH.CH O CI H3CH,CO (6) OH (d) (1) a. a b.b c.c d.d e. e f. f CHLB Br Which alkyl halide shown below would react the fastest under typical Snl conditions? HC CH; Br CHCHB HC Br (d) (...
5. Which of the following reagents is the best choice for the reaction shown below? CH Cн, A) H2O2 B) LAH C) POCI D) OsO E) O 6. Which of the following reagents can be used to convert cyclopentanol to cyclopentane? A) TOSCI, pyridine followed by LiAlH4 B) Na2Cr207, H2SO4 C) NaBH4 followed by H30 D) POClypyr, followed by H2, Pt E) both A and D 7. What is the product of the following reaction? OH Cro3, HC, pyridi ne...
would this E2 reaction go faster or slower than the ordinary bromocyclohexane. explain Which of the following shows the conformation necessary for E2 elimination of the compound shown below? SH І я t Br