Starting from cyclohexane make the following compounds. You must start with cyclohexane, but then you may use any other reagents you wish.(15 pt) CH3 CH3 HO CH3 CH3 OH
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- The correct sequence of reagents for the following conversion is: Br N T OH Br OH BrGiven the following reaction sequence: What are the reagents for reaction 4? A) NaNH2 followed by EtOH B) NaNH2 followed by MeBr C) NaNH2 followed by EtBrC(CH3)3 CN OH A в Reaction: Bromination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? CH3 H3C || H3C CH3 'N-C-CH3 'N' H3C-N-CH3 A B Reaction: Bromination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest?|
- Draw the most stable product formed in each of the reactions shown. Reaction (a) 2 ch NaOEt, EtOH A Draw the product of reaction (a). Select Draw |||||| Rings C H O MoreChoose the reagent(s) that would be most likely to complete this reaction. HBr (1 equiv) H2O2 HBr (1 equiv) HCI (1 equiv) C Br2 (1 equiv) RCO3H E Br Done A,The correct sequence of reagents for the following conversion is: Br -Br N ОН Br ОН
- Which is the major product of the following reaction? Br NaOEt EtOH A) B) 20 D) H OEt OEtChoose the reagent(s) that would be most likely to complete this reaction. HBr (1 equiv) H2O2 HBr (1 equiv) HCI (1 equiv) C Br2 (1 equiv) RCO3H Br E Dene A,What reactant and product types would be most appropriate for the reagents shown? H₂O Br₂ 000 00 a alkene/epoxide C d e alkene/2-bromoalcohol alkene/syn-1,2-dibromide alkene/anti-1,2-dibromide alkene/1,2-diol
- What reagents do you need to use to for the following reactions? Match the letter with the reagent! Remember in the answer boxes that: H2O = H₂O and H+ = H+ B с D OH OEt B C ? ? ? A [Choose ] [Choose ] [Choose ] [Choose ] OH D Me OHH2O, H* What is the major product? НО ОН OH OHWhat are the hemiacetal and acetal products of the reaction (s) shown below? H+ 1eq. CH₂OH hemiacetal H+ 1eq. CH3OH acetal