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- Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.Which one of the statements below is wrong about Zaitsev’s Rule. a. None of the above b. The Zaitsev’s Rule demonstrate the principle of regioselectivity in elimination reactions c. The more substituted alkene is the major product of E1 or E2 elimination d. The more substituted alkane product is obtained when a proton is removed from β-carbon that is bonded to the fewest hydrogens e. The most stable alkene is generally the major productWhy is this considered an Elimination E2 reaction? C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + water
- Select the member of each pair that shows the greater rate of SN2 reaction with KN3 in acetone.Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaFWhich halogen compound in each of the following pairs will react faster in SN2 reaction :(i) CH3Br or CH3I(ii) (CH3)3 C – Cl or CH3 – Cl
- Which alkyl bromide(s) can form the alkene under E2 elimination conditions.The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2
- Which mononitro product is the result of the nitration reaction of the compound whose open structure is given below? or consists of products? Show it.Complete the following reactions with the majority products and the missing reaction conditions. Indicate stereochemistry if applicable. Also indicate the type of reaction that took place (SN1, SN2, E1, E2, E1bc)Define the Reaction of Organometallic Reagents with Other Compounds ?