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- (b) Predict the suitable solvent (H2O or CH3COCH:) to increase the reaction of bromopropane (CH3CH2CH2B1) with sodium hydroxide (NaOH). Two reactions are shown below: NaOH, 55 °C CH;CH,CH,Br CH;CH,CH,OH + + NaBr H,O (i) NaOH, 55 °C CH;CH,CH,Br CH;CH,CH,OH + NaBr (ii) H,C- CH3Draw a structural formula for the major organic product of each reaction and specify the most likely mechanism by which each is formed.IV. Complete the equations for the following reactions. Show all organic alkene products form, mechanism, indicate the major product and the rule Ş(CH3)2 NaSH HEAT OH™ HEAT
- 6. Some reactions of 2-iodopropane are shown below: reaction 1 CH;CHCH; reaction 3 (CH3),CHOCH3 CH;CH=CH, reaction 2 (CH3)½CHNH, i) For each of the reactions shown, name the reagent used and state the condition of reaction. ii) State the type of mechanism of hydrolysis reaction in 2-iodopropane. iii) Write the mechanism involve in the reaction3Use catalysts and reagents that require the following reactions.
- 5. Consider the synthesis of 2-butanone from butyne: Hg2+ || CH3CH,-C=C–H CH;CH,-Ĉ-CH3 H3o* (iv) Name the class of compound D belongs to. (v) Comment on the stability of compound D compared to 3-butanone.Questão 10A certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis resulted in CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. What is the reasonable structure for this hydrocarbon? Hexadec-6,10-dino undec-1,5-dino Hept-1,5-dino hex-1,5-dino nahPleas don't provide handwritten solution .....
- 196. Subject : - ChemistryWhich of the following reactions will synthesize phenol from benzene? 1) HNO3 + H2SO4; 2) Fe, HCl; 3) NaNO2, HCl, 0-10 oC; 4) warm H2SO4 and H2O 1) HNO3 + H2SO4; 2) Fe, HCl; 3) NaNO2, HCl, 0-10 oC; 4) CuCN; 5) dilute acid and heat 1) Acetyl chloride & AlCl3; 2) bleach 1) Ph-N2+ + KI; 2) BrMgCH=CH2 in ether, followed by H3O+; 3) warm, conc'd KMnO4 1) Cl-CH(CH3)-CH2CH2CH3 + FeBr3; 2) hot, conc'd KMnO4From the table of available reagents select the one(s) you would use to convert:3-pentanol to 3-bromopentane:cyclopentanol to trans-2-methylcyclopentanol:Use the minimum number of steps; in no case are more than four steps necessary.List reagents by letter in the order that they are used; example: fa.