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- Which alkene is major product of the E2 reaction below? Options: 1 2 3 4Please show the mechanism with arrow formalism.3. For the following structures: CH3a C-CH,CH3 C Hy' H (a) Determine whether each radical is a primary, secondary, or tertiary radical. (b) Rank these radicals in terms of their relative stability (1 = most stable to 3 = least stable). 4 Draw the (2) banoggata 1o
- Which of the following would be the most reactive in a Diels-Alder [4+2] cycloaddition as the diene? 0000 2 = = - IV || ||| IVRank the following carbocations in order of decreasing stability, putting the most stable first. II Multiple Choice |> || > II Il >l> II III > T> || III > || > TIncluding reasonance structures, draw most stable allylic cation for both
- 2) Predict the major product for each reaction. Indicate correct stereochemistry. a. b. H3C H3C HO ||||| HO ||||| CH3 ||||| Br H Br CH3 H NaOH NaOH thrive qode-tums ng uboiqyWhich one of the following dienophiles is most reactive in the Diels-Alder reaction? || ON OI = || ||| • IV LOCH 3 VRank the alkenes shown below based on stability, should be indicated as (most stable (left) to least stable right): i.e.: A > B > C > D