Which best describes why carbocation formation is the rate determining step of a unimolecular substitution reaction? O The ABC step is slow. The nucelophile is too weak to attack without a carbocation present. The carbocation formed is unstable and high in energy. Carbocation formation is reversible so it doesn't readily occur. The solvent is acting as the nucleophile.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 8E
icon
Related questions
Question

please explain! 

Which best describes why carbocation formation is the rate determining step of a unimolecular
substitution reaction?
The ABC step is slow.
The nucelophile is too weak to attack without a carbocation present.
The carbocation formed is unstable and high in energy.
Carbocation formation is reversible so it doesn't readily occur.
The solvent is acting as the nucleophile.
Transcribed Image Text:Which best describes why carbocation formation is the rate determining step of a unimolecular substitution reaction? The ABC step is slow. The nucelophile is too weak to attack without a carbocation present. The carbocation formed is unstable and high in energy. Carbocation formation is reversible so it doesn't readily occur. The solvent is acting as the nucleophile.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Protection of Groups in Organic Synthesis
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning