Concept explainers
Videos
(a)
Interpretation:
The IUPAC name of the given molecule is to be written.
Concept introduction:
The root name of the molecule is the name of the
(b)
Interpretation:
The IUPAC name of the given molecule is to be written.
Concept introduction:
The root name of the molecule is the name of the alkane which depends on the longest continuous chain of carbon atoms. The name of the substituent attached to the parent chain is written as a prefix to the left side of the root. The chain is numbered such that the carbon atom to which the substituent is attached, gets the lowest possible number. This number is written on the left side of the substituent and separated by a hyphen.
(c)
Interpretation:
The IUPAC name of the given molecule is to be written.
Concept introduction:
The root name of the molecule is the name of the alkane which depends on the longest continuous chain of carbon atoms. The name of the substituent attached to the parent chain is written as a prefix to the left side of the root. The chain is numbered such that the carbon atom to which the substituent is attached, gets the lowest possible number. This number is written on the left side of the substituent and separated by a hyphen.
(d)
Interpretation:
The IUPAC name of the given molecule is to be written.
Concept introduction:
The root name of the molecule is the name of the alkane which depends on the longest continuous chain of carbon atoms. The name of the substituent attached to the parent chain is written as a prefix to the left side of the root. The chain is numbered such that the carbon atom to which the substituent is attached, gets the lowest possible number. This number is written on the left side of the substituent and separated by a hyphen.
Want to see the full answer?
Check out a sample textbook solution
Chapter A Solutions
Organic Chemistry: Principles And Mechanisms
- 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
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning