Predict the Major product(s) for the following reactions. Show the correct stereochemistry when needed!! (CH3)2NNa Ph substitution mechanism: mechanism: Br H₂O Δ elimination
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- CH3 to Br- -H + Nal • product; Sy2 product of the reaction is : Аcetone H- -CH3 CH2 – CH3 CH3 CH3 CH3 CH3 it it -H H- -CH3 (d) -CH3 -H- (а) H• (Ъ) H- -CH3 -CH3 (с) H- CH -H- ČH2 – CH3 ČH2 – CH3 CH2 – CH3 CH2- CH3 2.help with this(a) Rank the following carbocations in order of increasing electrophilicity (1 = lowest electrophilicity, 4 = highest electrophilicity). (b) Rank the following 1,1-halomethylcyclopentanes in order of reactivity in an SN1 reaction (1 = lowest reactivity, 4 = highest reactivity. CH3 CI B with SNI, nor reactive means more stable (c) Rank the following species in terms of increasing nucleophilicity in an SN2 reaction in a po aprotic solvent (1 = lowest nucleophilicity, 4 = highest nucleophilicity).
- For the following reactions, give the major product(s) formed. Show relevant stereochemistry. а) Br CH3OH 25°C b) HBr c) (E)– 3,4 – dimethyl – 3 – hexene H2 Pt d) 85% H3PO4 Н2О, 165°C онProvide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these steps.Give the Major product(s) and name the starting compound with stereochemistry: H2O H2O H2SO4 H,SO, HgSO,
- Draw the line structures of the products for a) and b) in the reactions below. No stereochenistry is required.6-46 Show how each compound might be synthesized by the SN2 displacement of an alkyl halide. SCH,CH, (a) -CH₂OH (c) (d) CHÍNH, 6-47 (a) Give twn synthecac fox (CI) qu (b) (e) H₂C=CH-CH₂CN n OLL BU (1) H-C=C-CH₂CH₂CH₂What product will be obtained for the below reaction: CH3 -? H;C-C=CH2 + I-CI CH3 CH3 (А) H;C-C-CH2-CI (В) H3C-C-CH,–I CI CH3 CH3 (С) H3C-C-CH3 (D) H;С—ҫ— СH, ČI
- Draw the structure of the major product of each reaction (If a racemic mixture is formed, indicate both enantiomers), and show the mechanismProvide the structure of the missing products or reactants. Show the relevant stereochemistry if necessary. H3C Br H₂O _SH [4© 1 product 2 products (2 isomers) ✓ OH + ?<When the alkene A was treated first with Hg(OAc)2 in MeOH and second with NaBH4 the product was the ether B. Using curved arrows please give the mechanism for the first step of (Hg(OAc)2 in MeOH) this reaction, including any regioselectivity or stereoselectivity. H3C 1. Hg(OAc)2, MeOH H3C O-CH3 =CH2 ✓ -CH3 H3C 2. NaBH H3C A B