
(a)
Interpretation:
The common name to the simple ester formed by a reaction between methanol and propionic acid is to be stated.
Concept introduction:
The reaction between acid and alcohol gives an ester as a major product. The ester group is derived by a
(b)
Interpretation:
The common name to the simple ester formed by a reaction between methanol and butyric acid is to be stated.
Concept introduction:
The reaction between acid and alcohol gives an ester as a major product. The ester group is derived by a carboxylic acid group in which the acidic hydrogen is replaced by an alkyl group. Esters are identified for their characteristic sweet smell.
(c)
Interpretation:
The common name to the simple ester formed by a reaction between methanol and lactic acid is to be stated.
Concept introduction:
The reaction between acid and alcohol gives an ester as a major product. The ester group is derived by a carboxylic acid group in which the acidic hydrogen is replaced by an alkyl group. Esters are identified for their characteristic sweet smell.

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Chapter 15 Solutions
Chemistry for Today: General Organic and Biochemistry
- Indicate the products obtained by mixing 2,2-dimethylpropanal with acetaldehyde and sodium ethoxide in ethanol.arrow_forwardSynthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forward
- Synthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forward
- Indicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forward
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