In SN1 reaction halide react with nucleophile. There are no base. So, option 1 and 2 are wrong.
In SN1 reaction, rate depends only on concentration of halide and not on concentration of nucleophile.
So, option 5 and 4 are wrong. This means option 3 is correct
Answer: option 3
What is the rate law for SN1 reaction? rate k[Base] rate k[RX][Base] rate k[RX] rate kinucleophile]...
What is the rate law for E2 reaction? rate = K[Base] rate = k[RX][Base] rate = K[RX] rate = k[nucleophile] rate = K[RX] [Nucleophile]
What is the rate law for E1 reaction? rate = k[Base] rate = K[RX][Base] rate = k[RX] rate = K[nucleophile) rate = k[RX][Nucleophile!
What is the rate law for E1 reaction? rate = k[Base] rate = K[RX][Base] rate = k[RX] rate = K[nucleophile) rate = k[RX][Nucleophile!
11. What is the rate law for the following SN1 reaction? +H2O
11. What is the rate law for the following Sn1 reaction? + H2O
For the chemical reaction answer the following questions: 1. Is the mechanism Sn1 or Sn2? 2. What kind of substrate reacts in the following reaction? (2 ° , 2 ° allylic , 3 ° ) 3. Is the role of the alkyl halide reactant an acid, base, electrophile, nucleophile , or both a nucleophile and base? 4. Is the role of the reagent KI an acid, base, electrophile, nucleophile , or both a nucleophile and base? 5. What is the...
Which of the following could represent the rate law for an SN1 reaction? a) Rate = k[A] b) Rate = k[A]2 c) Rate = k[A][B] d) Rate = k[A][B]2 e) Rate = k[A]2 [B]2 Please explain which is the correct answer and why? Thanks
2. Consider the Sn1 reaction shown below and answer the following questions. Br K . CHOH + CH3OH — Kºchs + HBr CH3 + HBr Ph Ph 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....
4. (5 pts) Complete the table comparing SN2 and SN1 reactions. SN2 SN1 rate k[R-XINuc] rate rate substrate reactivity methyl 1> 2 >> 3° polar, aprotic fastest stronger nucleophiles react faster solvent nucleophile inversion stereochemistry
Q1) Which compound will undergo SN1 reaction fastest? CI Cl Q2) What is true about SN1 reaction of alkyl halides? a) Reaction favored by non-polar solvents. b) Reaction rate depends on concentration of alkyl halide c) SN1 proceeds in one step thru transition state d) Reaction rate depends on concentration of nucleophile