(a)
Interpretation:
Balanced equation for the hydrogenation of 3,4-dichlorocycloheptene has to be written.
Concept Introduction:
Addition of hydrogen molecule to an unsaturated bond present in hydrocarbon is known as hydrogenation. During hydrogenation, the unsaturated bond present is broken and a carbon‑hydrogen bond is formed. Hydrogenation can be accomplished by use of metal catalyst such as platinum, nickel, or palladium. If an
Balanced equation is the one where the atoms of the same kind are equal on both sides of the chemical equation.
(b)
Interpretation:
Balanced equation for the halogenation of 3-methylcyclopentene has to be written.
Concept Introduction:
Addition of halogen molecule to an unsaturated bond present in hydrocarbon is known as halogenation. During halogenation, the unsaturated bond present is broken and a carbon‑halogen bond is formed.
Balanced equation is the one where the atoms of the same kind are equal on both sides of the chemical equation.
(c)
Interpretation:
Balanced equation for the hydration of cyclobutene has to be written.
Concept Introduction:
Addition of water molecule to an unsaturated bond present in hydrocarbon is known as hydration. During hydration, the unsaturated bond present is broken and a carbon‑hydrogen, carbon‑hydroxyl bond is formed.
Balanced equation is the one where the atoms of the same kind are equal on both sides of the chemical equation.
(d)
Interpretation:
Balanced equation for the hydrohalogenation of cyclohexene has to be written.
Concept Introduction:
Addition of hydrogen halide to an unsaturated bond present in hydrocarbon is known as hydrohalogenation. During hydrohalogenation, the unsaturated bond present is broken and a carbon‑hydrogen, carbon‑halogen bond is formed.
Balanced equation is the one where the atoms of the same kind are equal on both sides of the chemical equation.

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Chapter 11 Solutions
GENERAL,ORGANIC+BIOCHEM (LOOSELEAF)
- 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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