Concept explainers
(a)
Interpretation:
The structure for the given compound is to be drawn and its IUPAC name is to be written.
Concept introduction:
An
When writing the IPUAC name, if there are two possible roots, the root is chosen such that it has maximum number of substituents attached. The root is numbered such that the substituents attached get the lowest locant numbers. First, the substituents are written alphabetically with their respective locant numbers. The root name is written at the end. Two numbers are separated by a comma while a number and a word is separated by a hyphen.
(b)
Interpretation:
The structure for the given compound is to be drawn and its IUPAC name is to be written.
Concept introduction:
An alkane is said to be substituted if a hydrogen atom of the alkane is replaced by another atom or group of atoms. From the number of carbon atoms in the longest carbon chain the root name is identified. The names of the substituents and their respective locant numbers show the carbon atoms of the root to which the substituents are attached.
When writing the IPUAC name, if there are two possible roots, the root is chosen such that it has maximum number of substituents attached. The root is numbered such that the substituents attached get the lowest locant numbers. First, the substituents are written alphabetically with their respective locant numbers. The root name is written at the end. Two numbers are separated by a comma while a number and a word is separated by a hyphen.
(c)
Interpretation:
The structure for the given compound is to be drawn and its IUPAC name is to be written.
Concept introduction:
An alkane is said to be substituted if a hydrogen atom of the alkane is replaced by another atom or group of atoms. From the number of carbon atoms in the longest carbon chain the root name is identified. The names of the substituents and their respective locant numbers show the carbon atoms of the root to which the substituents are attached.
When writing the IPUAC name, if there are two possible roots, the root is chosen such that it has maximum number of substituents attached. The root is numbered such that the substituents attached get the lowest locant numbers. First, the substituents are written alphabetically with their respective locant numbers. The root name is written at the end. Two numbers are separated by a comma while a number and a word is separated by a hyphen.
(d)
Interpretation:
The structure for the given compound is to be drawn and its IUPAC name is to be written.
Concept introduction:
An alkane is said to be substituted if a hydrogen atom of the alkane is replaced by another atom or group of atoms. From the number of carbon atoms in the longest carbon chain the root name is identified. The names of the substituents and their respective locant numbers show the carbon atoms of the root to which the substituents are attached.
When writing the IPUAC name, if there are two possible roots, the root is chosen such that it has maximum number of substituents attached. The root is numbered such that the substituents attached get the lowest locant numbers. First, the substituents are written alphabetically with their respective locant numbers. The root name is written at the end. Two numbers are separated by a comma while a number and a word is separated by a hyphen.
(e)
Interpretation:
The structure for the given compound is to be drawn and its IUPAC name is to be written.
Concept introduction:
An alkane is said to be substituted if a hydrogen atom of the alkane is replaced by another atom or group of atoms. From the number of carbon atoms in the longest carbon chain the root name is identified. The names of the substituents and their respective locant numbers show the carbon atoms of the root to which the substituents are attached.
When writing the IPUAC name, if there are two possible roots, the root is chosen such that it has maximum number of substituents attached. The root is numbered such that the substituents attached get the lowest locant numbers. First, the substituents are written alphabetically with their respective locant numbers. The root name is written at the end. Two numbers are separated by a comma while a number and a word is separated by a hyphen.
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Chapter A Solutions
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
- Draw the structures of the following compounds. (a) trans-1-chloro-2-methylcyclohexanearrow_forwardWrite a complete chemical equation showing reactants, products, and catalysts needed(if any) for the following reaction and (2) Draw and name the organic compound found inevery reaction.(Use condensed structural formula) (A) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr(B) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide(C) Formation of Gilman reagent using isopropyl bromidearrow_forward(a) Write a chemical test to distinguish between: (i) Chlorobenzene and Benzyl chloride. (ii) Chloroform and Carbon tetrachloride. (b) Why is methyl chloride hydrolysed more easily than chlorobenzene?arrow_forward
- (a) (CH3)3CBr give the IUPAC name.arrow_forwardDraw a structure for each compound (includes old and new names).(a) 3-methylpent-1-enearrow_forwardGiven each of the IUPAC names provided, draw the corresponding structure. (a) 1-cyclopentylhexane;(b) cyclohexylcyclohexane; (c) 1,2-dicyclopropylnonanearrow_forward
- 2) Provide structures for the following compounds: a) ethyl acetate b) Pentanoic acidarrow_forwardDraw the structure of each of the following molecules. (a) pentanoic anhydride; (b) hexanoic propanoic anhydride; (c) ethanoic 3-methylpentanoic anhydridearrow_forward(a) Draw a specific organic reaction for the hydrohalogenation addition reaction of alkenes. (b) Also write the reagents involved in the reaction (c) and name and identify its major and minor product by writing its IUPAC name.arrow_forward
- Indicate whether each statement is true or false. (a) Alkanesdo not contain any carbon–carbon multiple bonds.(b) Cyclobutane contains a four-membered ring. (c) Alkenescontain carbon–carbon triple bonds. (d) Alkynes containcarbon–carbon double bonds. (e) Pentane is a saturatedhydrocarbon but 1-pentene is an unsaturated hydrocarbon.(f) Cyclohexane is an aromatic hydrocarbon. (g) The methylgroup contains one less hydrogen atom than methane.arrow_forwardDraw the structures of the following compounds. (a) chloroformarrow_forward(a) Draw a specific organic reaction for the hydration addition reaction of alkenes. (b) Also write the reagents involved in the reaction (c) and name and identify its major and minor product by writing its IUPAC name.arrow_forward
