
Concept explainers
(a)
Interpretation:
The IUPAC name for the given compound is to be determined.
Concept introduction:
For a molecule that has more than one double bond or triple bond, the IUPAC name must indicate the number of double bonds or triple bonds present as well as their locations. To name the molecule with multiple double/triple bonds, establish the root as the longest carbon chain or the largest carbon ring that contains the greatest number of entire
(b)
Interpretation:
The IUPAC name for the given compound is to be determined.
Concept introduction:
For a molecule that has more than one double bond or triple bond, the IUPAC name must indicate the number of double bonds or triple bonds present as well as their locations. To name the molecule with multiple double/triple bonds, establish the root as the longest carbon chain or the largest carbon ring that contains the greatest number of entire
(c)
Interpretation:
The IUPAC name for the given compound is to be determined.
Concept introduction:
For a molecule that has more than one double bond or triple bond, the IUPAC name must indicate the number of double bonds or triple bonds present as well as their locations. To name the molecule with multiple double/triple bonds, establish the root as the longest carbon chain or the largest carbon ring that contains the greatest number of entire

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Chapter B Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- 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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