The major product of the following reaction has the molecular formula C10H1603. Draw its structure in the most stable tautomeric form. 1. NaOC,H; 2. Н,О" С, Н,ОН
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- O In this step alkyne anion is alting and it is attacking cecting acting as 4 electrophile a Pla وعك Ho as a nucleophile on the genen molecule, which is Br pom 산 2-Bromo propane (26105 576 honros он 2The major product of the given reaction has the molecular formula C10H16O3. Draw its structure in the most stable tautomeric form.Draw the organic product(s) of the following reaction. CH3 H3C-C-CEC-H CH3 NaOC2Hs / CH5OH 1 eq. NANH2, NH3(1) CH;CH,CH,CH2-Br H-CEC-H H;C CH-Br H3C 1 eq. NaNH2, NH3() H3C-CEC-H
- Q5. What product is formed when cyclohexanone is reacted with each of the following reagents? MgBr KCN H30* H30 NABH4 H;O*Determine the structures of compounds A through D in the following reaction scheme: 1. NaH NaOH C H20 PBP3 A 2. D A 3. НWhat is the major organic product of the following reaction? 1. ВНз 2. Н-О2, НО- ОН O: II IV IV ||
- What is the major elimination product obtained from the following reaction? CH3 CH3 NaOCH₂CH3 HOCH₂CH3 Ot-Bu || CH3 Ot-Bu ||| CH3 IV CH33. Provide the mechanism going from a cyclohexenone to an a,ß-unsaturated carbonyl and a ketone. + H-OH RO, ROH, ADraw the product when each compound is treated with either (CH3)2CuLi, followed by H2O, or HC≡CLi, followed by 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.Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہMelamine, 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.