(a)
Interpretation:
The IUPAC name for the given compound is to be assigned.
Concept introduction:
In naming organic compounds, the
(b)
Interpretation:
The IUPAC name for the given compound is to be assigned.
Concept introduction:
In naming organic compounds, the functional groups other than the highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing a functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If ‘
Number the carbon chain in a way that the functional group and the substituents attached gets the lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.
(c)
Interpretation:
The IUPAC name for the given compound is to be assigned.
Concept introduction:
In naming organic compounds, the functional groups other than the highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing a functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If ‘amide’ is present as the highest priority group, suffix amide replaces ‘e’ from the parent chain name. The group attached to the N atom is written as a prefix to the root name with the letter ‘N’.
Number the carbon chain in a way that the functional group and the substituents attached gets the lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.
(d)
Interpretation:
The IUPAC name for the given compound is to be assigned.
Concept introduction:
In naming organic compounds, the functional groups other than the highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing a functional group. Remove the e from the normal ane, ene, or yne ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached gets the lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Want to see the full answer?
Check out a sample textbook solution
Chapter F Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- 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
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning


