The reaction of butanolc acid with methanol in the presence of HCl forms: butyl methanoate methyl...
QUESTION 1 Propanoyl chloride reacts with an acetate anion to give which product? Acetic propanoic anhydride propanoic acetic anhydride propyl acetate Cacetyl propanoate QUESTION 2 Reaction of benzoic acid with thionyl chloride produces compound A. Compound A is reacted with 2 moles of ammonia to give compound B which is then reacted with thionyl chloride to furnish compound C. Compounds C is then treated with NaOH in the first step and acidified with acid in the second step to give...
QUESTION 1 The reaction of butanoic acid with bromine in the presence of phosphorus tribromide followed by addition of water yields which product? 2,3-dibromobutanoic acid 3-chlorobutanoic acid C2-bromobutanoic acid C 2-chlorobutanoic acid QUESTION 2 What is the relationship between keto and enol tautomers? Cresonance forms stereoisomers constitutional isomers different conformations of the same compound QUESTION 3 The reaction of cyclohexanone with LDA followed by allylbromide gives which product? C2-allylcyclohexanone C1-allylcyclohexanol C3-allylcyclohexanone C2-lithium diisopropylamidecyclohexanone
QUESTION 1 Reaction of pentanoic acid with thionyl chloride produces compound B followed by addition of two equivalents of ammonia to produce which compound? butanamide ammoniumpentanoic acid pentanamide CN-pentylamine QUESTION 2 Pentanoic acid reacts with lithium aluminum hydride followed by water to produce compound B. Compound B is reacted with phosphorus tribromide to give compound C which is then treated with sodium cyanide to produce compound D. Finally, compound D is reacted with lithium aluminum hydride and water to give...
A reaction was performed in which 3.022 g of benzoic acid was reacted with excess methanol to make 1.1 g of methyl benzoate. Calculate the theoretical yield and percent yield for this reaction.
Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2-methoxy-2-methylbutane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
5. The equilibrium constant (K) for the formation of methyl benzoate from methanol and benzoic acid at 25°C is 3.77. Use the equation for the equilibrium constant to calculate the theoretical yield of methyl benzoate for the following conditions. (6 marks) a) With equal initial amounts of the reactants (1 mole of each reactant) b) With a threefold (x 3) excess of methanol (1 mole of benzoic acid and 3 moles of methanol) 6. Suggest a chemical reaction (include structures...
Use curved arrows to propose mechanisms for the following reaction (a)Propene with HCl (b)tert-butylbromide with methanol(c)3-methyl-2-pentene with chlorine (d)3-methyl-1-butene with sulphiric acid(e)Propyne with excess HBr (f)2-Pentyne with water in the presence of a mineral acid.
a. 1. Sketch the reaction coordinate diagram for the solvolysis of t-butyl chloride with water, labeling the maxima and minima with appropriate structures (including the intermediate and transition states). Assume the overall reaction is exothermic. 2. Draw the product of the reaction of t-butyl chloride with each of the following solvents Methanol b. Ethanol c. 2-propanol 3. The Lucas Test and Jones Test (Jones Oxidation) are both chemical test for the presence of alcohols. Please view the videos on the...
Question 1 --/1 ) Reaction of 2-cyclohexenone with hydrazine in the presence of potassium hydroxide furnishes which product? 1 cyclohexanone © cyclohexene 3 3-hydrazone-1-cyclohexene 4 3-hydrazone-3-cyclohexanone Question 2 ( --/1) Treatment of 5-oxohexanal with one molar equivalent of ethylene glycol and catalytic acid gives preferentially which general compound? (1) Protection of both ketone and aldehyde 2 Protection of only aldehyde 3 Protection of only ketone a No reaction since the equilibrium favors the reactants Question 3 (--/1) Reaction of triphenylphosphine...
In the boxes provided, draw the structures of the four intermediates and the organic product when the following compound is reacted with methanol in the presence of acid in a Fischer esterification reaction. You don’t have to show the important resonancestructures.I need to see the mechanism to get the answers.