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- Draww the products of each reduction reactionThe key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.
- Which compound is the dominant product in the reaction shown below? KMNO4 .COOH (A) H*/H,O (B) COOH .COOH (C) (D) HOOC HOOC Compound B Compound C Compound D Compound AGive the major product of the following reaction. CI AlCl3, heat Zn(Hg), HCI heat ? There is no reaction under these conditions or the correct product is not listed here.Please assign the correct letter to each reaction.
- Draw all of the substitution and elimination products formed from thegiven alkyl halide with each reagent: (a) CH3OH; (b) KOH. Indicate thestereochemistry around the stereogenic centers present in the products,as well as the mechanism by which each product is formed.Draw all the products of this reduction reaction: H₂N NIR H3C CH3Draw the reaction and choose the correct characterizations
- Is the reagent for all elimination reactions conc. H2SO4? or just the reactions ones with OH?For alkenes A, B, and C: (a) Rank A, B, and C in order of increasing heat of hydrogenation; (b) rank A, B, and C in order of increasing rate of reaction with H2, Pd-C; (c) draw the products formed when each alkene is treated with ozone, followed by Zn, H2O.4. What are the products obtained from the following elimination reaction? Indicate the major product. CH;CH2CCH3 H2O CI 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion in an elimination reaction. CH;CH,CH,CH,CCH3 Br b) For the major elimination product obtained in 5a), which stereoisomer (cis or trans) is obtained in greater yield? Draw the two isomers and provide the names of the compounds.