Ans : III < II < I
The primary carbocations are less stable than secondary and tertiary ones.
The tertiary carbocations are the most stable carbocations.
The reason of this stability behavior can be explained on the basis of hyperconjugation and donation of electrons from the neighbouring carbon atoms.
Rank the following radicals in order of increasing stability, putting the least stable first.
Rank the carbocation in order of increasing stability, putting the least stable first .
Arrange the following radicals in order of increasing stability (least stable to most stable) Arrange the following radicals in order of increasing stability (least stable to most stable). Least stable Most stable
Rank the following carbocations in increasing order of stability. (1 = least stable) 3. (5 points) Rank the following carbocations in increasing order of stability. (1 = least stable) eg og Å
Rank the following radicals in order of decreasing stability (most stable to least stable 11 III TV III > I > I > IV III > | > | > IV Ill > IV> || >1 IV>]> || > III II >> III > IV
2. Rank the following radicals in decreasing order of stability (1-most stable, 5-least stable): CH2 CH3 (CH3)2Ć (CH3)2CH CH3CH2
3. (8 pts) Utilizing the boxes below, rank the following radicals in order of increasing stability. Below the boxes, fully explain the reasoning behind the ranking. CH3 А в со Least Stable Least Stable O O O O Most Stable Most stable
11. Arrange the following radicals in order of increasing stability (where 1 -least stable and 4- most stable). Explain your reasoning. Sob to Explain your reasoning:
Rank the following carbocations in order of increasing stability. “1” is the least stable, “4” is the most stable or ot an CH3 or
Arrange the following radicals in order of increasing stability, with 1 being the least stable and 7 being the most stable.23.1 (3).png23.1 (2).png23.1 (1).png
Rank the following carbocations in order of increasing stability. “l” is the least stable, “4” is the most stable. (2 pts) or od ano CH3