Concept explainers
(a)
Interpretation:
The systematic name for each isomer has to be given.
Concept introduction:
The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
Prefix: Represents the substituent present in the molecule and its position in the root name.
Suffix: Denotes the presence of
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(b)
Interpretation:
The common name for each isomer has to be given.
Concept introduction:
The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
Prefix: Represents the substituent present in the molecule and its position in the root name.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(c)
Interpretation:
The number of primary
Concept introduction:
The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
Prefix: Represents the substituent present in the molecule and its position in the root name.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(d)
Interpretation:
The number of secondary alkyl halide has to be given.
Concept introduction:
The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
Prefix: Represents the substituent present in the molecule and its position in the root name.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
(e)
Interpretation:
The number of tertiary alkyl halide has to be given.
Concept introduction:
The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.
The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.
Prefix: Represents the substituent present in the molecule and its position in the root name.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkynes molecules, suffix will be ‘yne’.
Root word represents the longest continuous carbon skeleton of the organic molecule.
Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.
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Organic Chemistry, Books a la Carte Edition (8th Edition)
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- Show how to prepare each compound from 2-methyl- 1- propanol. a. 2- methylpropene b. 2- methyl- 2- propanol c. 2- methylpropanoic acid (CH3)2CHCOOHarrow_forward62. Catenation is a property of the carbon atom which describes its ability to A. bond with other carbon atoms B. form double and triple bonds C. exist in molecules in plant and animal form D. form bonds in its ground state E. share valence electrons with non-polar species 63. The transformation of methane to carbon tetrachloride is an example of A. an electrophilic addition B. a free-radical substitution C. a nucleophilic addition D. an electrophilic substitution E. a unimolecular substitution reaction 64. In the addition of HX (where X is a halogen) to a double bond, the hydrogen atom goes to the carbon that already has more hydrogens. This general observation is given and summarized by A. Hund's rule B. Markovnikov's rule C. Huckel's rule D. Zaitsev's rule E. Cahn-Ingold-Prelog rule 65. Which of the following statements about the carbonyl group of ketones and aldehydes is (are) true? 1. It can attract nucleophiles. II. It can attract electrophiles. III. It tends to undergo addition…arrow_forwardShow how to convert 1- Butene into these compounds. a. Butane b. 2- Butanol c. 2- Bromobutane d. 1,2- Dibromobutanearrow_forward
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning