
Concept explainers
(a)
Interpretation:
Physical state at room temperature for unbranched saturated monocarboxylic acid that contains four carbon atoms has to be indicated.
Concept Introduction:
Physical property of
(b)
Interpretation:
Physical state at room temperature for unbranched saturated dicarboxylic acid that contains four carbon atoms has to be indicated.
Concept Introduction:
Physical property of carboxylic acid is decided by the carbon chain and the functional group. Carboxylic acids are highly polar, as the carboxyl group is more polar. Due to this polar nature, the melting and boiling point are very high. Monocarboxylic acids that are unsubstituted which contains up to nine carbon atoms are present in liquid state. They have very sharp odor. Monocarboxylic acids that have more than ten carbon atoms in an unbranched fashion are waxy solids. They do not have any odor because of low volatility. Similar to this, dicarboxylic acids and aromatic carboxylic acids do not have any odor and they are solids.
(c)
Interpretation:
Physical state at room temperature for unbranched saturated monocarboxylic acid that contains five carbon atoms has to be indicated.
Concept Introduction:
Physical property of carboxylic acid is decided by the carbon chain and the functional group. Carboxylic acids are highly polar, as the carboxyl group is more polar. Due to this polar nature, the melting and boiling point are very high. Monocarboxylic acids that are unsubstituted which contains up to nine carbon atoms are present in liquid state. They have very sharp odor. Monocarboxylic acids that have more than ten carbon atoms in an unbranched fashion are waxy solids. They do not have any odor because of low volatility. Similar to this, dicarboxylic acids and aromatic carboxylic acids do not have any odor and they are solids.
(d)
Interpretation:
Physical state at room temperature for unbranched saturated dicarboxylic acid that contains six carbon atoms has to be indicated.
Concept Introduction:
Physical property of carboxylic acid is decided by the carbon chain and the functional group. Carboxylic acids are highly polar, as the carboxyl group is more polar. Due to this polar nature, the melting and boiling point are very high. Monocarboxylic acids that are unsubstituted which contains up to nine carbon atoms are present in liquid state. They have very sharp odor. Monocarboxylic acids that have more than ten carbon atoms in an unbranched fashion are waxy solids. They do not have any odor because of low volatility. Similar to this, dicarboxylic acids and aromatic carboxylic acids do not have any odor and they are solids.

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Chapter 16 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
- Synthesize 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_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol 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_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Indicate 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_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate 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_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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