The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, are due to

+1 vote
135 views
asked Aug 28, 2017 in JEE by Ranjit (3,065 points) 10 55

The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, are due to

(A) σ→p (empty) and  σ→π electron delocalisations

(B) σ→σ and σ→π electron delocalisations

(C) σ→p (filled) and σ→π electron delocalisations

(D) p (filled) →σ→π electron delocalisations

1 Answer

+3 votes
answered Aug 28, 2017 by Annu Priya (18,055 points) 24 46 95
selected Sep 1, 2017 by Abhishek Kumar
 
Best answer

Correct answer:
image

Explanation:

commented Aug 28, 2017 by Ranjit (3,065 points) 10 55
Oh Thanks.....It's JEE ADVANCE 2013 QUESTION

Related questions

0 votes
0 answers
+1 vote
1 answer
asked Aug 28, 2017 in JEE by Ranjit (3,065 points)
0 votes
0 answers

Welcome to Sarthaks eConnect: A unique platform where students can interact with teachers/experts/students to get solutions to their queries. Students (upto class 10+2) preparing for All Government Exams, CBSE Board Exam, ICSE Board Exam, State Board Exam, JEE (Mains+Advance) and NEET can ask questions from any subject and get quick answers by subject teachers/ experts/mentors/students.

One Thought Forever

“There is a close connection between getting up in the world and getting up in the morning.“
– Anon
~~~*****~~~

...