List the following carbocations in each set in order from most stable (numbering from 1) to...
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. 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...
Please explain the solution for each step! Rank the carbocations in order from most stable (I) to least stable (5). momeð
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.
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.
2. Rank the following carbocations in order from least stable to most stable THEN justify your answer thoroughly in words A B C D
Rank the following carbocations in order of increasing stability. “1” is the least stable, “4” is the most stable or ot an CH3 or
Circle the most stable and underline the least stable carbocations. 1.(1 pt each) Circle the most stable and underline the least stable carbocations below. 3- a.
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
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