Question

Explain why C0 = [H+]∞ for the solvolysis reaction of t-butyl chloride and water

Explain why C0 = [H+] for the solvolysis reaction of t-butyl chloride and water

Homework Answers

Answer #1

t-butyl chloride hydrlysis is a Sn1 type of reacton. The mechanism involves loss of Cl- in the first step which is the rate determining slow step of the reaction. The formed tertiary carbocation is stable and gets solvolyzed in water. The solvolysis is the second step and is performed by the solvent water which is in excess. The second step is the fast step and does not influence the rate of the reaction, making the concentration Co = [H+]inifnity (exces solvent) does not influence rate of the reaction and its concentration remains almost unchanged at all times.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Explain why the reaction of 1,4-di-t-butylbenzene with t-butyl chloride and AlCl3 gives 1,3, 5-tri-t-butylbenzene
Explain why the reaction of 1,4-di-t-butylbenzene with t-butyl chloride and AlCl3 gives 1,3, 5-tri-t-butylbenzene
Explain the relative reactives of the butyl chloride, sec-butyl chloride, and tert-butyl chloride with ethanolic AgNO3...
Explain the relative reactives of the butyl chloride, sec-butyl chloride, and tert-butyl chloride with ethanolic AgNO3 in term of the structure of the transition state
Prepare energy diagrams for the hydrolysis of tert-butyl chloride with two different concentrations of water. Explain...
Prepare energy diagrams for the hydrolysis of tert-butyl chloride with two different concentrations of water. Explain any significant differences in the diagrams and how they affect the reaction rate.
Write a rational mechanism for the conversion of t-butyl alcohol into t-butyl chloride using appropriate reagents
Write a rational mechanism for the conversion of t-butyl alcohol into t-butyl chloride using appropriate reagents
Draw (clearly and legibly) the seven reactions for 1-bromobutane, 1-chlorobutane, 2-bromobutane, 2-chlorobutane, t-butyl bromide, t-butyl chloride,...
Draw (clearly and legibly) the seven reactions for 1-bromobutane, 1-chlorobutane, 2-bromobutane, 2-chlorobutane, t-butyl bromide, t-butyl chloride, and bromobenzene in an SN2 reaction with 15% NaI in acetone.
1) Use the integrated rate law to calculate the concentration of tert-butyl chloride at t =...
1) Use the integrated rate law to calculate the concentration of tert-butyl chloride at t = ( 1.5) X (half life) if half life is 23.5 seconds 2) Explain why the rate can't be determined simply examining the balanced equation? 3) propose an experiment to determine the activation energy of this reaction
which appears to have the greatest effect on the hydrolysis of t-butyl chloride: concentration of the...
which appears to have the greatest effect on the hydrolysis of t-butyl chloride: concentration of the alkyl halide or concentration of NaOH? Why?
The experiment was the synthesis of t-butyl chloride which used magnesium sulfate as a reagent. a)Why...
The experiment was the synthesis of t-butyl chloride which used magnesium sulfate as a reagent. a)Why did you use it? b)What effect would you see in the IR spectrum if you did not use enough magnesium sulfate?
Upon reacting 1,4-di-t-butylbenzene with aluminum trichloride and t-butyl chloride, the main product formed is 1,3,5-tri-t-butylbenzene due...
Upon reacting 1,4-di-t-butylbenzene with aluminum trichloride and t-butyl chloride, the main product formed is 1,3,5-tri-t-butylbenzene due to the demand of the t-butyl group. What best explains this phenomenon? (Hint: This is still essentially a Freidel-Crafts reaction; think about the mechanism of alkylation.)
experiment ( preparation of tert-butyl chloride ) 1- what is the purpose of washing tert-butyl chloride...
experiment ( preparation of tert-butyl chloride ) 1- what is the purpose of washing tert-butyl chloride with saturated NaHCO3 solution ? 2- why should the distillation be ice-cold ?
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT