Welcome Guest Search | Active Topics |

Tag as favorite
Prep101 Practice Sets: Class 4, Question 3
Options
Previous Topic Next Topic
Josh_4080
#1 Posted : Monday, June 22, 2020 5:26:35 PM
Rank: Advanced Member

Groups: Registered
Joined: 3/18/2019
Posts: 30

Thanks: 0 times
Was thanked: 0 time(s) in 0 post(s)
I found this question hard because it required really understanding the mechanisms of saponification. If I forgot a mechanism on the MCAT, would there be another way to solve this problem? For example, how would you be able to predict if something has a tetrahedral intermediate? Or, how would I go about determining the mechanism if I did not know it.

Thanks!
Back to top
Report?
INSTR_Katerina_102
#2 Posted : Thursday, June 25, 2020 8:38:37 PM
Rank: Advanced Member

Groups: Registered
Joined: 6/24/2019
Posts: 250

Thanks: 0 times
Was thanked: 0 time(s) in 0 post(s)
Is this the extra practice reaction package? With the protonated carboxylic acid and methoxid?

This would go through a tetrahedral intermediate, it's just not explicitly stated in the answer.

Pretty all nucleophilic acyl substitutions (those with acid chlorides and anhydrides, carboxylic acids etc) go through a tetrahedral intermediate, while Sn1 and Sn2 type reactions do not.

Sometimes we get lazy as chemists though and we don't draw the tetrahedral intermediate because it takes so much time (sadly me).

Please let me know if I have the wrong question!
Back to top
Report?
Users browsing this topic
Guest (2)
Tag as favorite
You cannot post new topics in this forum.
You cannot reply to topics in this forum.
You cannot delete your posts in this forum.
You cannot edit your posts in this forum.
You cannot create polls in this forum.
You cannot vote in polls in this forum.

Clean Slate theme by Jaben Cargman (Tiny Gecko)
Powered by YAF | YAF © 2003-2009, Yet Another Forum.NET
This page was generated in 0.073 seconds.