Select the mechanism(s) where the concentration of the nucleophile/base has no effect on the reaction rate.
In SN2 and E2 reactions rates are altered with the presence of strong nucleophile/base is used in the reaction.
In SN1 and E1 reaction, the rate is dependent on the slowest step that is the formation of the carbocation hence the slowest path will determine the rate of the reaction.
Hence the reaction is independent of nucleophile/base concentration in the case of E1 and SN1 reactions.
Hence the correct answer is A and C
Select the mechanism(s) where the concentration of the nucleophile/base has no effect on the reaction rate.
Select the mechanism(s) where the concentration of the nucleophile/base has no effect on the reaction rate.
Select the mechanism(s) where the concentration of the nucleophile has no effect on the reaction rate. Select the mechanism(s) where the concentration of the nucleophile has no effect on the reaction rate. SN1 SN2 E1 E2
Which mechanism(s) listed below generally proceed(s) smoothly when a low concentration of neutral nucleophile base is used in the presence of a polar protic solvent? O a. Sy2 b. Syl and El c. El d. E2 e. Si f. Sn2 and E2
How does halving the nucleophile concentration affect the rate of an E2 reaction? Select the single best answer. o no change O rate halved O rate quadrupled o rate doubled
a)indicate the reaction mechanism(s) favored by the particular type of leaving group, substrate, nucleophile/base, and solvent employed; b) predict the major pathway(s) that will occur under these conditions; c) provide the structure(s) of the major product(s) of the reaction ко Ме Me HT H Br Me-N Ме., 'H Me ко Ме Me HT H Br Me-N Ме., 'H Me
For a certain substitution reaction, the rate of substitution is found to be independent of both the concentration and the nature of the nucleophile. What is the most likely mechanism? For a certain substitution reaction, the rate of substitution is found to be independent of both the concentration and the nature of the nucleophile. What is the most likely mechanism?
What is the effect of the first step in the acid-catalyzed reaction mechanism shown? Select all responses that apply. General mechanism: Acidic conditions - H-A -H + :A® R Y LG * H-Nu - LG - H Nu RDS öHAO ÖH a ñ =Rt LG / Corant) Nu Rtió + MÃ . solvent) u® H ÖH op + 1 nocor OH H-LG e s Stre-H + ÄⓇ = RP R ALG o -H+A - R . Nu it solvent) H-LG...
Which substitution elimination pathway(s) is(are) favored by a high concentration of the attacking species (nucleophile base)? a. Sy2/E2 b. Sy2 O CE2 d. Syi e. El f. SNIE1
strong nucleophile weak base strong bulky base strong nucleophile strong base Promote SN2/E2 weak nucleophile weak base Promote SN1/E1 Promote SN2 Promote E2 CH Br HS NCT HO CHO CHÚCHO NaNO NaOH NOME Noe HOORS Conjugate acids have pka 16-18 Conjugate acids Recall, you make hydroxide have pka 11 or alkoxide ons from the corresponding alcohol or water and Nat CH,OH (MOH) HO CH,CH,OH (EXOH) | HC-Ć-o to CH tert-BUOK NOCH KOHBU NEOBU The structures above are all ways of...
How does doubling the concentration of both the alkyl halide and the nucleophile affect the rate of the above S N1 reaction?