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- 23) Which reaction will yield the following alkene as only elimination product? NaOEt A) Br E-3- Br NaOCH, B) KOIBU "Br KHSOJAT D) 24) What is the product of the following transformation? AgOH Br A) B) OH C) D) OH 25) Rank the following alkenes according to their heat of combustion from the LOWEST to the HIGHEST. II II IV A) II < IV < I< III B) III < I< IV < || C)I< || < IV < IIl D) II < IV < |I < IWhen an alkene is treated with Hg(OAc)2 in EtOH, followed by reaction with basic NaBH4, what functional group is formed? alkane ether O syn diol O alkyne O epoxideDraw the structure of the products formed in the following reactions. a) CN H,0, H* CH3 он b) H3C- -CI + CH3 c) CH3 KMNO4, A, H,O" CH3 d) Br Mg, éther CO, H*
- why H2SO4 has a positive reaction with cyclohexene?How many alkenes could you treat with H2, Pd/C to prepare methylcyclopentane?9. Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H20, H2SO4; or [2] BH3 followed by H2O2, "OH. A io onutouTC.rvinmmoo ewo ebyoleen.g er besibhoyn motis M doso al waH s b. a. Seblaar molsHsno isq onol nose 2eob isticho to eqyt ewni.d Cnistnoo ennug 29ob anodogle yoam woH.o O bns 18 to alnemala erlT nertw bemot witam-S ae doue anexie leohtemmyeni
- Draw the alkene that would react with the reagent given to account for the product formed. ? + H₂O ● You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. 8 H₂SO4 // CH3 CH3CHCCH3 OH CH3 ? [F Previous Email InstructAs a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect to oxidize faster, cis-4-tert-butylcyclo-hexanol or trans-4-tert-butylcyclohexanol? Draw the more stable chair conformation of each molecule.Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.
- Which alcohol will form the most stable carbocation? CH3 a) CH;CHCH,OH CH3 b) CH—сон CH3 c) - OH d) CH;OH O a O b O d Organic compounds that contain terminal carbonyl group. ketone aldehyde ether alcoholDraw the major product of the reaction between 1-butanol and Na2Cr207, H2SO4, H2O. O, O, e CHWhat is the major product formed when 3-methyl-1-butene is treated with Hg(C2H3O2)2 in a THF/ethanol mixture followed by NaBH4 in base?