Order these carbocations from most stable (1) to least stable. (5) If there is resonance, that can make the carbocation more stable than if there isn't; for example, primary benzylic is more stable than primary allylic, which is more stable than secondary, as a general rule.
Explanation :
benzylic carbo cation is most stable among the all .
the order of carbo cations from most to least stable :
benzylic > allylic > tertiary > secondary > primary .
A = benzylic
B = tertiary
C = primary
D = allylic
E = secondary
Order these carbocations from most stable (1) to least stable. (5) If there is resonance, that...
Rank the following allylic carbocations in order from least stable to most stable THEN justify your answer in words: For each of the following pairs of compounds, circle the one that is the stronger acid: Which one of the following is the MOST stable carbocation? Circle the correct answer.
List the following carbocations in each set in order from most stable (numbering from 1) to least stable (numbering to 3): PLEASE EXPLAIN! primary, secondary, tertion least 2) (3 points) List the following carbocations in each set in order from most stable (numbering from 1) to least stable (numbering to 3): a. CH3CH2CCH CH3CH2CHCH2 CH3CH2CH2CH2 CHE b. CH3CHCHCH; CH3CHCHCH2 CH3CHCHCH? CH3
1. Rank the following carbocations in order from most stable (1) to least stable (4). o ó no 8 2. Consider the following carbocation. Would this carbocation undergo a rearrangement? If so, show the mechanism (curved arrows) for the rearrangement (including the rearranged cation that is the product of your curved arrows) and explain why it happens. If not, explain why it would not rearrange.
1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. 2. Rank the following free radical intermediates in order of increasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. CH2 bro ledo IV b III 10 112TV ] 21 3. 2,3-Dimethylbutane reacts with bromine in the presence of light to give a monobrominated product....
2. Carbocation stability: Rank the following carbocations from the most stable to the least stable. + (a) (b) (c) (d)
Rank the following carbocations in order of decreasing stability. Most Stable Least Stable Least Stable
Rank the following carbocations in order of decreasing stability. Most Stable Least Stable Least Stable
14. Place 1º, 2º, 3º and Methyl carbocations in order from least stable to most stable. What factor(s) account for the stability of the most stable species?
2. Rank the following carbocations in order from least stable to most stable THEN justify your answer thoroughly in words A B C D
east stable most stable The following are three examples of the relative stability of carbocations in your answer to question 2. Each of these reactions should show a relatively stable carbocation intermediate. (a) The two-step reaction of 1-methylcyclohexene with HBr follows the Markovnikov 3. rule. (b) Choose 1-butanol or tert-butyl alcohol to undergo a 3-step reaction with HBr to form the alkyl bromide. The second step is the S1 formation of a carbocation. (c) Show the one most stable resonance...