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- Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Write the products for (A-I). Label products with the mechanism (Sn2, Sn1, E1, E2) that produced it and write out and label major vs minor elimination products.3-Bromocyclohexene is a secondary halide, and benzyl bromide is a primary halide. Both halides undergo SN1 substitution about as fast as most tertiary halides. Use resonance structures to explain this enhanced reactivity.
- Provide a reasonable mechanism for the transformation illustrated below.What sequence of reagents can be used to accomplish the conversion shown below?1. Which of the following is the strongest nucleophile? Refer to the diagram below with an MeOH, MeSH, etc. 2. Which of the following is true about the stereochemistry of SN1 reaction?a.retention of configuration at the electrophilic centerb.50:50 mixture of retention and inversion of configuration at the electrophilic centerc.inversion of configuration at the electrophilic centerd. slightly more inversion than retention at the electrophilic center
- Which of the following reagent best accomplish this transformation below? a. BH3, THF, H2O2 b. NaNH2, NH3 c. H2SO4, H2O, HgSO4 d. H2, LindlarWhy is this considered an Elimination E2 reaction? C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + waterProvide the synthetic route for the following reaction? (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2
- Determine the reagents A, B, C, D, E and the structure of compounds I, II, II in the reaction belowSeveral reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.Please show the mechanisms that convert compound 1 into compound 2. Thank you!