(a)
Interpretation:
The structure of the molecule that corresponds to the IUPAC name
Concept introduction:
The IUPAC name of a compound consists of three parts, prefix, root, and suffix. The root is the longest continuous carbon chain or the largest ring that bears the highest priority functional group. The suffix refers to the highest priority functional group. The functional group name suffix replaces the last ‘e’ in the root alkyl/aryl name. The root chain or ring carbons are numbered so that the highest priority group gets the lowest possible location numbers. The number is inserted between the root and the suffix unless redundant. Any other, low priority
The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the
(b)
Interpretation:
The structure of the molecule that corresponds to the IUPAC name
Concept introduction:
IUPAC name of a compound consists of three parts, prefix, root, and suffix. The root is the longest continuous carbon chain or the largest ring that bears the highest priority functional group. The suffix refers to the highest priority functional group. The functional group name suffix replaces the last ‘e’ in the root alkyl/aryl name. The root chain or ring carbons are numbered so that the highest priority group gets the lowest possible location numbers. The number is inserted between the root and the suffix unless redundant. Any other low priority functional groups are listed alphabetically in the prefix, along with the location numberss. A prefix di, tri, etc. is used in case two or more instances of the functional group are present.
The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group.
(c)
Interpretation:
The structure of the molecule that corresponds to the IUPAC name
Concept introduction:
IUPAC name of a compound consists of three parts, prefix, root, and suffix. The root is the longest continuous carbon chain or the largest ring that bears the highest priority functional group. The suffix refers to the highest priority functional group. The functional group name suffix replaces the last ‘e’ in the root alkyl/aryl name. The root chain or ring carbons are numbered so that the highest priority group gets the lowest possible location numbers. The number is inserted between the root and the suffix unless redundant. Any other low priority functional groups are listed alphabetically in the prefix, along with the location numbers. A prefix di, tri, etc. is used in case two or more instances of the functional group are present.
The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group.
(d)
Interpretation:
The structure of the molecule that corresponds to the IUPAC name
Concept introduction:
IUPAC name of a compound consists of three parts, prefix, root. and suffix. The root is the longest continuous carbon chain or the largest ring that bears the highest priority functional group. The suffix refers to the highest priority functional group. The functional group name suffix replaces the last ‘e’ in the root alkyl/aryl name. The root chain or ring carbons are numbered so that the highest priority group gets the lowest possible location numbers. The number is inserted between the root and the suffix unless redundant. Any other, low priority functional groups are listed alphabetically in the prefix, along with the location numbers. A prefix di, tri, etc. is used in case two or more instances of the functional group are present.
The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group.

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Chapter E Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- Please help me solve this reaction.arrow_forwardIndicate 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_forward
- Synthesize 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_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- If 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_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forward
- We 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_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
