
Concept explainers
(a)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction: The group that contains carboxyl group which is attached to at least one hydrogen is said to be an
In order to give the name to the aldehyde group, the following steps are followed:
1. The parent (longest)
2. The ending of the parent chain from alkane (-e) is changed to -al for an aldehyde group. The carbonyl group of an aldehyde appear at the end of the carbon chain so, the numbering start with carbon having aldehyde group.
3. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
(b)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction: The group that contains carboxyl group which is attached to at least one hydrogen is said to be an aldehyde group, general representation of an aldehyde group is RCH=O or RCHO. Whereas the group that contains carboxyl group which is attached to two carbon atoms is said to be a
In order to give the name to the ketone group, the following steps are followed:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -one for a ketone group.
3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.
4. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
(c)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction: The group that contains carboxyl group which is attached to at least one hydrogen is said to be an aldehyde group, general representation of an aldehyde group is RCH=O or RCHO.
In order to give the name to the aldehyde group, the following steps are followed:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -al for an aldehyde group. The carbonyl group of an aldehyde appear at the end of the carbon chain so, the numbering start with carbon having aldehyde group.
3. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec

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Chapter 17 Solutions
Basic Chemistry
- 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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