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- ORGANIC CHEMISTRY - PERICYCLIC REACTIONS Draw the mechanism, explain the stereochemistry of the products, indicate the type of reaction.What is the reaction? cycloaddition A A B D [Single selection] A B D CO₂Me CO₂Me HPh HPh OH CO₂Me CO₂Mes 2req 2req 2req 2req 2req Visited Complete the equation for the following reaction by drawing a structural formula for the missing organic product. Onomorecom NH3 CH₂ + You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • Draw cations and anions in separate sketchers. Ⓒ%81 CH₂ H₂O ? Y Jn [1
- didentify the Allowry reactions, as substitution, elimination, or addition DrawWelection arrows to show how the in each reactors Circle and identify any reactive bands break & form intermediates of carbon. Ħ Br Br → AH-Br →→ → XB²(8) + он он H30+ H NaоH, H₂0 25° C NAOH catalytic amountThe following Wittig reactions may produce a mixture of alkene stereoisomers. Write the products for each of the reactions and indicate the stereoisomers if any. || Ph,P CH3 + ? (1) LOME (2) R N. Ph,P=CH,R' Me
- Consider the following mechanism of reaction: CH3 CH, CH3 CH;C CH, + H-CI CH;CCH, + C: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic HCl and CI" are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI" are both electrophilic The alkene and CI" are both nucleophilic AMeving to another question will save this responseThe order from most reactive to least reactive with aqueous ammonia is (А) CH--o-č-CH, * CH,--oCH,CH, * CH,--a CH--č-OCH,CH, ° CH,--c³ CH---o-č-CH, > CH3-C-OCH2CH3 | CH3-C-CI | (В) %3D > CH3-C-CI CH3-C-0-C-CH3 (C) > CH3-C-CI CH3-C-OCH2CH3 CH3-C-0-C-CH3 (D) || > CH3-C-CI CH3-C-0-C-CH3 CH3-C-OCH2CH316 What is X in the following reaction? * (i) X CH,-C=C-CH, (ii) H+/Zn CH,-C-C-CH, HNO3 02 03 KMN04 None of the above
