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A: Step 1: Step 2: Step 3: Step 4:
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Q: Show mechanism..don't give Ai generated solution
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A: Step 1: Step 2: Step 3: Step 4:
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- Draw the products formed when attached compound is treated with HNO3 and H2SO4. State whether the reaction occurs faster or slower than a similar reaction with benzene.Draw a stepwise mechanism for the following substitution. Explain why 2-chloropyridine reacts faster than chlorobenzene in this type of reaction.What reaction took place in the reaction below? CHẠCH, CH; CH,(CH),CH; CH{CH,),C-OCH; CHẠCH)A CH; CHỊCHCo H0 НОСН CH/CH),CH, CH, (CH),C-C HOCH, HH O reduction (hydrogenation) O amide synthesis O acetal hydrolysis O ester synthesis O acid base O dehydration O thioester synthesis O phosphate ester synthesis O hydration O ester hydrolysis O amide hydrolysis O oxidation O acetal synthesis
- Finish the indicated reaction by filling in and starting materials, reagents or products as needed a) b) c) d) type type OEt type SN ₂ HI ether Br₂, H₂O alkere in a) NaOEt/EtOH b) neutralize type elimination Ixp a) cH₂ B‹ b) NaOH you c) aq. malonic Ester Synthesis aq, HCl OHDraw the step-by-step mechanism using curved arrows of the following reaction in acidic condition.