How does doubling the concentration of both the alkyl halide and the nucleophile affect the rate of the above S N1 reaction?
SN1 reaction rate only depends on the concentration of the alkyl halide as in the slow step the carbocation formation occurs. The rate is unimoecular or first order in the alkyl halide.
So, doubling the concentration of alkyl halide will increase the rate 2 times but doubling the concentration of nucleophile will not affect the rate.
How does doubling the concentration of both the alkyl halide and the nucleophile affect the rate...
Assuming no other changes, what is the effect of doubling only the concentration of the alkyl halide in the above S_N 1 reaction? quadruples the rate rate is halved no change triples the rate doubles the rate
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
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
9. How does doubling the concentration of hydroxide (OH-) and halve the concentration of bromomethane (CH3Br) in the following reaction affect the rate of the reaction? CH3BE + HO CH3OH + Br A) no change B) doubles the rate C) triples the rate D) quadruples the rate E) rate is halved
(12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide or via acyl substitution reactions. Show the compounds required to synthesize the ester two different ways. Be sure the product will be favored. 4. H0 alkyl halide nucleophile acyl derivative nucleophile Given the information in the question above, provide appropriate reactants above. hat does a nucleophilic substitution reaction look like in general? Acyl substitution? (12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide...
c. The reaction of triphenylphosphine with an alkyl halide is a bimolecular nucleophilic substitution (SN2) reaction in which triphenylphosphine is the nucleophile and the alkyl halide is theelectrophile. Is triphenylphosphine acting like a Lewis acid, Lewis base, Bronsted-Lowry acid, orBronsted-Lowry base? How would you characterize the behavior of the alkyl halide? d. In the lab, you will make your ylide by reacting benzyltriphenylphosphonium bromide with sodium hydroxide. How would you characterize this reaction? e. Is the ylide that you form...
Experiment 1 Comment on Structure and Formula Alkyl Halide Name Nucleophile Time (min) to relative reaction Precipitate rates of alkyl halides wwte preci pi tote 2. whte vii. cl chloro min nprecipi tote ci benzul 0 Secs preci p tate Experiment 2 Comment on Alkyt Halide Name Structure and Time (min) to relative reactivity Precipitate of the leaving NucleophileT Formula group white vin prei p min whi te Ci Do reactidi no 咐ano Post Lab Questions- Experiment 5-SN2 Reactions 1....
predict the major organic product formed in the following reaction alkyl halide nucleophile CH, e) H Br KOBu" HOBu Br Н CH Br CH,CH,OH two products formed 8 + CHI h) Br NaOCH H
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary, Label the nucleophile as strong or weak. Decide whether an S2 or an Sol reaction occurs. Alter, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol + Na CH₂ CH OH b. Reaction of 2-bromopropane in ethanol Br + CH.CH, OH - c. Reaction of (R) 3-chloro-3-methylheptane in acetic acid CH3...
consider the Sn1 reaction shown below and answer the following questions. Br Br + CH3OH CH3 + HBO A. Write the rate law for the reaction. B. Identify the nucleophile, the electrophile, and the reaction solvent. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of the alkyl halide. b. Increasing the concentration of CH3OH. c. Replacing HOCH3 with NaOCH3. d. Changing the alkyl halide from a bromide to an...