
elimination/substitution reactions TsO. он 1. TsCl, pyr 2. NaN Ph н. CH3 NaOH Н,с E2 Only...
1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. CH-Oн heat NaOCHs + HBr HG OH Nal Hо acetone NaBr +HBr 2. Predict which reactions proceeded by an SN1, SN2, El or E2 mechanism: NaOCH CH +NaBr оснCH Носн,сн, 50° +NaCl Nal DMSO, 45 Br NaOCHa +NaBr +HOCH Носн, 100° но +HI acetone, 50 HSO +HO HO,...
1 Br NaBr NaOH HO сHз CH3 Нс — она 2. Hао Нассн, CH3 a Proton transfer Radical chain addition d g E2 Elimination h SNl Nucleophilic substitution b Lewis acid/base e Electrophilic addition i S2 Nucleophilic substitution c Radical chain substitution f= E1 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers 1. 2 Submit Answer Retry Entire Group 8 more group...
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a - Proton transfer dSN2 Nucleophilic substitution b- Lewis acid/base e-Electrophilic aromatic substitution c=E2 elimination f= g Nucleophilic subs at carbonyl(acyl Xfer) h-Conjugate (nucleophilic) addn r-carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a i for your answers. 1. 2.
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a -...
Question 1 The following reaction between 2-methylbut-2-ene and hydrogen bromide (HBr) is best described as what type of reaction? Refer to the Figure A) Addition B) Substitution C) Elimination D) Rearrangement Question 2 For the reaction in question 1, two products are possible- a major product, and a minor product. For the minor product, what is the splitting pattern for the added hydrogen (highlighted in red) that would be observed in the molecules HINMR spectrum? Refer to the Figure HBr...