based on the strength of the base and the type of alkyl
halide and the possible products are as follows
7-11 pls What reaction happens? SN1/SN2/E1/E2 And what are the products? Br Br NaCl DMSO ?...
1-6 What reaction happens? SN1/SN2/E1/E2 And what are the products? Naci DMSO OY ? NaoMe -BOK 11. NaOE Moet ? NaSH ?
Draw the major product and label as SN2, SN1, E2, or E1 7. Draw the major products of the following reactions, and label the reaction as SN2, SN1, E2 E1. (Darkly shaded bonds are wedged) Br NaOMe NaCN H2SO4 OTs NaSH OTs H20 NaOMe Br KOtBu OH HBr HBr OH
Draw the products of the following reaction and identify the following as SN1, SN2. For letters G and H. NaOH DMSO g. OB Br NaCN h. 2.. Draw the products of the following reaction and label the follow SN2, E1 or E2 reaction. { HEAT FAVORS ELIMINATION}(18 poi 0BN is a bulty hindved proton C 30 carbau so v CH3 CI DBN a. El el Br NaOEt, heat - NaBv Na08t isa protic solvcut ad involee Ad cliuinitiar Readrans b....
describe each as Sn1, Sn2, E1 and E2 then draw a curved arrow mechanism for each reaction. NaSH DMSO SH KOH HO DMSO Br NANH NH3 OTs NH TsO TsO CHs CH3 Nal CH3 acetone CH O O
determine whether the reaction is Sn1, Sn2, E1 or E2 & draw the major product Br Me TH NaOET Me H D Br EtOH Me Ph
Analyze then draw the expected products of each of the following. Determine if it’s E1/E2/Sn1/Sn2 Br #5 OMs tBuOH OMs KOtBu DMSO OMs NaCN OMs
Determine if the reaction is SN1, SN2, E1, E2 and draw the product Br 9 11Go (ej AObo H20
Show the mechanism below for the reaction. figure out if its a sn1, sn2, e1 or e2 reaction in the process. Br NAOH
Q1. Identify the reaction mechanism most likely to take place (E1, SN1, E2, SN2 or a combination of these) in each of the following cases. Draw the major product(s), include stereochemistry when relevant. Br -OtBu Br NaCN, DMF → CI Носна 1. Nal/acetone 2. NaCN/DMF NaoMe H2SO4 OH Lyon CN (CH3)2CO CI NaOH →
Predict the most likely reaction mechanism (SN1, SN2, E1, E2) and draw all products. Nato=CH₂ E2 ran Br major 2. Draw complete mechanism with arrows for the SN1/E1 mechanism. Check for carbocation rearrangements. CH3 SMI 애 + H₂O7