Which will be the product(s) of the reaction. Select all that apply. CH3 NaSCHE - Bro...
Which will be the product(s) of the reaction. Select all that apply. CH3 Na SCH Bro Нас CH3 CH3 H3CCH3 CH3 SCH3 H5C CH3 CH3 CH3 о" CH3 Нас CH3 CH3 CH3 CH₃
Which will be the product(s) of the below reaction. Select all that apply. Br HOCH CH3 OCH2CH3 OCH2CH3
How does changing the alkyl halide from CH3CH2Br to (CH3)2CHBr affect the rate of an E2 reaction? Select the single best answer. O rate decreases O rate fluctuates O rate increases no change
What is/are the product(s) for the following reaction? Select all that apply. What is are the products for the following reaction Select all that apply. 1.03 2. DMS | HH
Nhat are the product(s) expected in the following reaction: H3C NaNH2 CI- CH3 NH3 b. C. d. H3C H2N H2C H3C H2N- C1- CI -CH3 -CH3 -CH3 -CHANH H2N
28) The reaction of tert-butyl bromide, (CH,)CBr, with ethanol affords the substitution product tert-butyl ethyl ether, (CH)1COCH CH, in acidic conditions. What would happen to the rate of the reaction if the concentration of ethanol was doubled? A) The rate remains the same. B) The rate decreases by a factor of 2 C) The rate increases by a factor of 2. D) The rate increases by a factor of 4. Circle the following alkyl halide that will undergo the fastest...
Select which compound is the most reactive in an SN1 reaction Br Select one: O III Assuming no other changes, what is the effect of doubling both the alkyl halide and the nucleophile concentrations in the reaction below? for OH 79 + HB Select one: O a quadruples the rate b. triples the rate c. doubles the rate O d. no change e. rate is halved B. Select which compound is the most reactive in an SN 1 reaction Sel...
Which of the following would increase the proportion of a substitution reaction that proceeds via a $ 2 mechanism, rather than S, 1? (choose all correct answers) Use a less reactive nucleophile. Use a more highly substituted alkyl halide. Increase the concentration of the alkyl halide. Increase the concentration of the nucleophile Which of the following reactions would most likely proceed via a SN 1 mechanism? (choose all correct answers) + CH3OH Br + HO- Br + CN + HBr...
2. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (primary, secondary, or tertiary alkyl halide), nucleophile (strong or poor), and the solvent type (protic or aptrotic). Specify the type of reaction mechanism (SN1 or SN2), show the curved arrow mechanism and draw the products as 3D structures to illustrate stereochemistry. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (1º, 2º, or 3 alkyl halide). mucleophile (strong or poor),...
which change(s) to this reaction system would increase the rate of reaction? select all that apply. CO+H2O --> CO2+H2 addition of catalyst addition of CO addition of CO2 lowering the temperature addition of H2