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An illustration depicts the fifteen reactions with acetone as the reactant. In the first reaction, hydrate formation, acetone reacts with water in acidic conditions to form a diol with the SMILES string CC(C)(O)O. In the second reaction, acetal formation, acetone reacts with alcohol in acidic condition, loses water, and forms an acetal and the SMILES string of general formula of acetal is CC(C)(O[R])O[R]. In the third reaction, cyclic acetal formation, acetone reacts with ethane diol in acidic conditions, loses water, and forms cyclic acetal with the SMILES string CC1(C)OCCO1. In the fourth reaction, cyclic thioacetal formation, acetone reacts with ethane dithiol in acidic condition, loses water, and forms cyclic thioacetal with the SMILES string CC1(C)SCCS1. In the fifth reaction, desulfurization, acetone reacts with ethane dithiol in acidic condition, loses water, and forms cyclic thioacetal with the SMILES string CC1(C)SCCS1. Cyclic thioacetal further is reduced by Raney nickel to propane. In the sixth reaction, imine formation, acetone reacts with primary amine in acidic condition, loses water, and forms an imine with SMILES string C/C(C)=N/[R]. In the seventh reaction, enamine formation, acetone reacts secondary amine in acidic condition, loses water, and forms an enamine with SMILES string C=C(C)N([R])[R]. In the eighth reaction, oxime formation, acetone reacts with hydroxyl amine in acidic condition, loses water, and forms oxime with SMILES string C/C(C)=N/O. In the ninth reaction, hydrazone formation, acetone reacts with hydrazine in acidic condition, loses water, and forms a molecule with SMILES string C/C(C)=N/N. This molecule further undergoes tenth reaction, Wolf-Kishner reduction, by hydrolysis in the presence of sodium hydroxide, water, and heat to form propane. In the eleventh reaction, reduction of a ketone, acetone reacts with lithium aluminum hydride and hydronium ion to form secondary alcohol with SMILES string CC(C)O. In the twelfth reaction, Grignard Reaction, acetone reacts with Grignard reagent, R M g B r, and hydronium ion to form secondary alcohol with SMILES string CC(C)(O)[R]. In the thirteenth reaction, cyanohydrin formation, acetone reacts with potassium cyanide and hydrochloric acid to form cyanohydrin with SMILES string CC(C)(O)C#N. In the fourteenth reaction, Wittig Reaction, acetone reacts with phosphorus ylide to form 2-methyl-1-propene with SMILES string C=C(C)C. In the fifteenth reaction, Baeyer-Villiger reaction, acetone reacts with peroxy acid to form ester with SMILES string COC(C)=O.
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Directions: Click the "Next" button below to access an interactive drag and drop version of this graphic, which will help reinforce the concepts you have been studying.

An illustration depicts the fifteen reactions with acetone as the reactant. In the first reaction, hydrate formation, acetone reacts with water in acidic conditions to form a diol with the SMILES string CC(C)(O)O. In the second reaction, acetal formation, acetone reacts with alcohol in acidic condition, loses water, and forms an acetal and the SMILES string of general formula of acetal is CC(C)(O[R])O[R]. In the third reaction, cyclic acetal formation, acetone reacts with ethane diol in acidic conditions, loses water, and forms cyclic acetal with the SMILES string CC1(C)OCCO1. In the fourth reaction, cyclic thioacetal formation, acetone reacts with ethane dithiol in acidic condition, loses water, and forms cyclic thioacetal with the SMILES string CC1(C)SCCS1. In the fifth reaction, desulfurization, acetone reacts with ethane dithiol in acidic condition, loses water, and forms cyclic thioacetal with the SMILES string CC1(C)SCCS1. Cyclic thioacetal further is reduced by Raney nickel to propane. In the sixth reaction, imine formation, acetone reacts with primary amine in acidic condition, loses water, and forms an imine with SMILES string C/C(C)=N/[R]. In the seventh reaction, enamine formation, acetone reacts secondary amine in acidic condition, loses water, and forms an enamine with SMILES string C=C(C)N([R])[R]. In the eighth reaction, oxime formation, acetone reacts with hydroxyl amine in acidic condition, loses water, and forms oxime with SMILES string C/C(C)=N/O. In the ninth reaction, hydrazone formation, acetone reacts with hydrazine in acidic condition, loses water, and forms a molecule with SMILES string C/C(C)=N/N. This molecule further undergoes tenth reaction, Wolf-Kishner reduction, by hydrolysis in the presence of sodium hydroxide, water, and heat to form propane. In the eleventh reaction, reduction of a ketone, acetone reacts with lithium aluminum hydride and hydronium ion to form secondary alcohol with SMILES string CC(C)O. In the twelfth reaction, Grignard Reaction, acetone reacts with Grignard reagent, R M g B r, and hydronium ion to form secondary alcohol with SMILES string CC(C)(O)[R]. In the thirteenth reaction, cyanohydrin formation, acetone reacts with potassium cyanide and hydrochloric acid to form cyanohydrin with SMILES string CC(C)(O)C#N. In the fourteenth reaction, Wittig Reaction, acetone reacts with phosphorus ylide to form 2-methyl-1-propene with SMILES string C=C(C)C. In the fifteenth reaction, Baeyer-Villiger reaction, acetone reacts with peroxy acid to form ester with SMILES string COC(C)=O.
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An illustration depicts fifteen reactions with acetone as the reactant. In the first reaction, hydrate formation, acetone reacts with unknown reagents to form a diol with the SMILES string CC(C)(O)O. In the second reaction, acetal formation, acetone reacts with unknown reagents to form an acetal and the SMILES string of general formula of acetal is CC(C)(O[R])O[R]. In the third reaction, cyclic acetal formation, acetone reacts with unknown reagents to form cyclic acetal with the SMILES string CC1(C)OCCO1. In the fourth reaction, cyclic thioacetal formation, acetone reacts with unknown reagents to form cyclic thioacetal with the SMILES string CC1(C)SCCS1. In the fifth reaction, desulfurization, acetone reacts with unknown reagents to form cyclic thioacetal with the SMILES string CC1(C)SCCS1. Cyclic thioacetal further is reduced by unknown reagents to form propane. In the sixth reaction, imine formation, acetone reacts with unknown reagents to form an imine with SMILES string C/C(C)=N/[R]. In the seventh reaction, enamine formation, acetone reacts unknown reagents to form an enamine with SMILES string C=C(C)N([R])[R]. In the eighth reaction, oxime formation, acetone reacts with unknown reagents to form oxime with SMILES string C/C(C)=N/O. In the ninth reaction, hydrazone formation, acetone reacts with unknown reagents to form a molecule with SMILES string C/C(C)=N/N. This molecule further undergoes tenth reaction, Wolf-Kishner reduction, with unknown reagents to form propane. In the eleventh reaction, reduction of a ketone, acetone reacts with unknown reagents to form secondary alcohol with SMILES string CC(C)O. In the twelfth reaction, Grignard Reaction, acetone reacts with unknown reagents to form secondary alcohol with SMILES string CC(C)(O)[R]. In the thirteenth reaction, cyanohydrin formation, acetone reacts with unknown reagents to form cyanohydrin with SMILES string CC(C)(O)C#N. In the fourteenth reaction, Wittig Reaction, acetone reacts with unknown reagents to form 2-methyl-1-propene with SMILES string C=C(C)C. In the fifteenth reaction, Baeyer-Villiger reaction, acetone reacts with unknown reagents to form ester with SMILES string COC(C)=O. The unknown reagents are represented by empty rectangular boxes.
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