During the synthesis of Ferrocene, deprotonation of cyclopentadiene is carried out using 1,...

Question:

During the synthesis of Ferrocene, deprotonation of cyclopentadiene is carried out using 1, 2-dimethoxyethane (DME). If the deprotonation is carried out using MeOH, will the reaction be faster or slower? Why?

Protic and Aprotic Solvents:

Polar organic solvents can be classified as either protic or aprotic. Protic solvents such as water, ethanol, and ammonia all have O-H or N-H bonds and can participate in hydrogen bonding. They can be proton accepting or proton donating, which may interfere with specific reactions. Aprotic solvents on the other hand cannot form hydrogen bonds with themselves.

Answer and Explanation: 1

Become a Study.com member to unlock this answer!

View this answer

DME, the solvent that is used in the deprotonation of cyclopentadiene, is polar aprotic. If the deprotonation is carried out using methanol, the...

See full answer below.


Learn more about this topic:

Loading...
Synthesis: Definition & Meaning

from

Chapter 5 / Lesson 3
16K

Synthesizing different pieces of information can add a new perspectives or even opinions to the original texts. Learn the meaning and definition of synthesis and examples of this process in literature and writing.


Related to this Question

Explore our homework questions and answers library