Concept explainers
(a)
Interpretation:
The given statement is true or false should be determined.
The IUPAC name of an alkene is derived from the name of the longest carbon chain that contains the carbon-carbon double bond.
Concept Introduction:
The IUPAC name is the set of rules that is created and applied by the International Union of pure and Applied Chemistry to generate systematic proper name of chemical compounds. This nomenclature is used to describe and identify the type and position of
Cis-trans stereoisomerisms are seen in alkenes compounds. Due to presence of two different groups bonded to carbon of carbon-carbon double bond, restricted action occurs in it and results into cis-trans isomerism. If same groups are present on the same side, then the isomer is called as cis-isomer and the same groups are present on different side the isomer is called as trans-isomer.

Answer to Problem 11P
The given statement is true.
Explanation of Solution
As per general rules of
(b)
Interpretation:
The given statement is true or false should be determined.
The IUPAC name of
Concept Introduction:
The IUPAC name is the set of rules that is created and applied by the International Union of pure and Applied Chemistry to generate systematic proper name of chemical compounds. This nomenclature is used to describe and identify the type and position of functional groups, side chains, double or triple bonds etc. in alphabetical order to provide systematic name to compound.
Alkenes are the compounds with very weak London dispersion forces and are nonpolar. They contain same skeleton structure and physical properties like alkanes but liquid at room temperature.
Cis-trans stereoisomerisms are seen in alkenes compounds. Due to presence of two different groups bonded to carbon of carbon-carbon double bond, restricted action occurs in it and results into cis-trans isomerism.
If same groups are present on the same side, then the isomer is called as cis- isomer and the same groups are present on different side the isomer is called as trans- isomer.

Answer to Problem 11P
The given statement is false.
Explanation of Solution
IUPAC name of
Therefore, the given statement is false.
(c)
Interpretation:
The given statement is true or false should be determined.
2-Methyl-2-butene shows cis-trans isomerism.
Concept Introduction:
The IUPAC name is the set of rules that is created and applied by the International Union of pure and Applied Chemistry to generate systematic proper name of chemical compounds. This nomenclature is used to describe and identify the type and position of functional groups, side chains, double or triple bonds etc. in alphabetical order to provide systematic name to compound.
Alkenes are the compounds with very weak London dispersion forces and are nonpolar. They contain same skeleton structure and physical properties like alkanes but liquid at room temperature.
Cis-trans stereoisomerisms are seen in alkenes compounds. Due to presence of two different groups bonded to carbon of carbon-carbon double bond, restricted action occurs in it and results into cis-trans isomerism.
If same groups are present on the same side, then the isomer is called as cis- isomer and the same groups are present on different side the isomer is called as trans- isomer.

Answer to Problem 11P
The given statement is false.
Explanation of Solution
2-Methyl-2-butene contains two methyl groups present on carbon atom of carbon-carbon double bond other carbon contains also methyl group.
To get cis and trans isomers, two different groups should be present on the carbon atoms of the carbons with double bond.
Thus, the statement is false.
(d)
Interpretation:
The given statement is true or false should be determined.
1,2-dimethylcyclohexene shows cis-trans isomerism.
Concept Introduction:
The IUPAC name is the set of rules that is created and applied by the International Union of pure and Applied Chemistry to generate systematic proper name of chemical compounds. This nomenclature is used to describe and identify the type and position of functional groups, side chains, double or triple bonds etc. in alphabetical order to provide systematic name to compound.
Alkenes are the compounds with very weak London dispersion forces and are nonpolar. They contain same skeleton structure and physical properties like alkanes but liquid at room temperature.
Cis-trans stereoisomerisms are seen in alkenes compounds. Due to presence of two different groups bonded to carbon of carbon-carbon double bond, restricted action occurs in it and results into cis-trans isomerism.
If same groups are present on the same side then the isomer is called as cis- isomer and the same groups are present on different side the isomer is called as trans- isomer.

Answer to Problem 11P
The given statement is false.
Explanation of Solution
Following are the structures of the isomers of 1,2-dimethylcyclohexane. Form this, we can see that all four atoms of carbon-carbon double bond are lying in same plane.
Therefore, the given statement is false.
(e)
Interpretation:
The given statement is true or false should be determined.
The IUPAC name of
Concept Introduction:
The IUPAC name is the set of rules that is created and applied by the International Union of pure and Applied Chemistry to generate systematic proper name of chemical compounds. This nomenclature is used to describe and identify the type and position of functional groups, side chains, double or triple bonds etc. in alphabetical order to provide systematic name to compound.
Alkenes are the compounds with very weak London dispersion forces and are nonpolar. They contain same skeleton structure and physical properties like alkanes but liquid at room temperature.
Cis-trans stereoisomerisms are seen in alkenes compounds. Due to presence of two different groups bonded to carbon of carbon-carbon double bond, restricted action occurs in it and results into cis-trans isomerism.
If same groups are present on the same side then the isomer is called as cis- isomer and the same groups are present on different side the isomer is called as trans- isomer.

Answer to Problem 11P
The given statement is true.
Explanation of Solution
The IUPAC name of
(f)
Interpretation:
The given statement is true or false should be determined.
1,3-Butadiene has two carbon-carbon double bonds and 22 =4 stereoisomers are possible for it.
Concept Introduction:
The IUPAC name is the set of rules that is created and applied by the International Union of pure and Applied Chemistry to generate systematic proper name of chemical compounds. This nomenclature is used to describe and identify the type and position of functional groups, side chains, double or triple bonds etc. in alphabetical order to provide systematic name to compound.
Alkenes are the compounds with very weak London dispersion forces and are nonpolar. They contain same skeleton structure and physical properties like alkanes but liquid at room temperature.
Cis-trans stereoisomerisms are seen in alkenes compounds. Due to presence of two different groups bonded to carbon of carbon-carbon double bond, restricted action occurs in it and results into cis-trans isomerism.
If same groups are present on the same side, then the isomer is called as cis- isomer and the same groups are present on different side the isomer is called as trans- isomer.

Answer to Problem 11P
The given statement is false.
Explanation of Solution
Following is the structure of 1,3-Butadiene. There are no stereocenters are present in the structure of 1,3-Butadiene. There should be presence of different groups for isomerism.
Therefore, the given statement is false.
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Chapter 12 Solutions
EP INTRO.TO GENERAL,ORGANIC...-OWL ACCE
- Fina x | Sign X Sign X lab: X Intro X Cop) X a chat x My x Grad xLaur x Laur x a sheg X S Shoj XS SHE X acmillanlearning.com/ihub/assessment/f188d950-dd73-11e0-9572-0800200c9a66/d591b3f2-d5f7-4983-843c-0d00c1c0340b/f2b47861-07c4-4d1b-a1ee-e7db27d6b4ee?actualCourseld=d591b3f2- 5 © Macmillan Learning Organic Chemistry Maxwell presented by Macmillan Learning For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product, showing the stereochemistry clearly. H H KOH Br EtOH Heat Select Draw Templates More Erase // C H Q Search hp Q2 Q Δ קו Resouarrow_forwardIs the structural form shown possible given the pKa constraints of the side chains?arrow_forwardon x Fina X Sign X Sign x lab X Intro X Cop X chat X My x Grac x Laur x Laur x ashes x S Shox S SHE x a eve.macmillanlearning.com/ihub/assessment/f188d950-dd73-11e0-9572-0800200c9a66/d591b3f2-d5f7-4983-843c-0d00c1c0340b/f2b47861-07c4-4d1b-a1ee-e7db27d6b4ee?actualCourseld=d591b3f2-c stions estion. ct each urces. +95 Macmillan Learning Draw the product formed by the reaction of potassium t-butoxide with (15,25)-1-bromo-2-methyl-1-phenylbutane (shown). Clearly show the stereochemistry of the product. H BH (CH3)3CO-K+ +100 H3CW (CH3)3COH +85 H3CH2C +95 ossible ↓ Q Search Select Draw Templates More C H 0 bp A Erase 2Q 112 Resouarrow_forward
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