April 24, 2024, 03:30:00 AM
Forum Rules: Read This Before Posting


Topic: Reaction rates question  (Read 2687 times)

0 Members and 1 Guest are viewing this topic.

Offline G O D I V A

  • Regular Member
  • ***
  • Posts: 48
  • Mole Snacks: +2/-1
Reaction rates question
« on: November 13, 2009, 05:58:18 AM »
Consider:

(1) (CH3)3CBr + CH3OH (in methanol)

and

(2) (Ph)CBr(CH3)2 + CH3OH (in methanol, solvent) -- (Thats 2-bromo-2-phenylbutane)

At 25 celcius and after 1 hour, which reaction will produce more of the substitution product?


I'm not understanding that.  Is the "substitution product" the product; i.e. (1) would be H2C=C(CH3)2 and (2) would be 2-phenyl-2-butanol?

How would I determine which would be faster?

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: Reaction rates question
« Reply #1 on: November 14, 2009, 05:08:52 AM »
I'm not understanding that.  Is the "substitution product" the product; i.e. (1) would be H2C=C(CH3)2 and (2) would be 2-phenyl-2-butanol?

No, neither of those are the correct products.

For (1), you have given an elimination product, and for (2) you have assumed the presence of water, which is not given in the question.

Look up nucleophilic substitution in your textbook, or google it, and decide which mechanism is operating in each case (SN1 or SN2).

Once you work out which mechanism is operating, you can work out the products and which reaction is faster.


My research: Google Scholar and Researchgate

Sponsored Links