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Prepare the following compound starting from an
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- Provide the correct product(s) for the following reactionTertiary alkyl halides will react by E2 under neutral conditions under acidic conditions under basic conditions will not react by E2Explain why α-pyrone reacts with Br2 to yield a substitution product (likebenzene does), rather than an addition product to one of its C=C bonds.
- Give a clear explanation of how the followingcarbocation is stabilized:The reaction below is classified as: a) substitutionb) eliminationc) additiond) rearrangementExplain why α-pyrone reacts with Br2 to yield a substitution product (like benzene does), rather than an addition product to one of its C=C bonds.
- Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Determine reagents C and D from the reaction scheme below.Provide a reasonable arrow-pushing mechanism for Reaction 5b, and explain the the stereochemical outcome. 5d below