The correct increasing order of acidity of the following
alkynes
(1) CH₃ -C ≡ C -CH₃
(2) CH₃ -C ≡ CH
(3) CH ≡ CH
(a) 1 < 2 < 3 (b) 2 < 3 < 1
(c) 3 < 2 < 1 (d) 1 < 3 < 2
Answers
Answer:
CH≡CH in which triple bond (≡) exists between two carbon atoms. Group of answer choices CH3CH3CH2 CH3CHCH2 More than one response is correct. Write a mechanism for the following reaction using arrows to show the electron movement for each step of the reaction.
The correct answer to the increasing order of the acidic strengths of the given compounds is - HCOOH > CH₃COOH > CH₃CH₂COOH. The strengths of the carboxylic acids are known to vary based on the total power to withdraw electrons of the atoms that are bonded to the carboxyl group.
For example, CH₃CH₂CH=CH-C≡CH is pent-3-en-1-yne. Your suggested name would be correct if the stereochemistry was defined though - well spotted! So this particular alkyne right here has alkyl groups on either side of my triple bond. So it's a disubstituted alkyne, and the more common term.
please mark as a brainlist answer