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.
Want to see more full solutions like this?
Chapter 12 Solutions
EP INTRO.TO GENERAL,ORGANIC...-OWL ACCE
- Li+ is a hard acid. With this in mind, which if the following compounds should be most soluble in water? Group of answer choices LiBr LiI LiF LiClarrow_forwardQ4: Write organic product(s) of the following reactions and show the curved-arrow mechanism of the reactions. Br MeOH OSO2CH3 MeOHarrow_forwardProvide the correct IUPAC name for the compound shown here. Reset cis- 5- trans- ☑ 4-6- 2- 1- 3- di iso tert- tri cyclo sec- oct but hept prop hex pent yl yne ene anearrow_forward
- Q6: Predict the major product(s) for the following reactions. Note the mechanism (SN1, SN2, E1 or E2) the reaction proceeds through. If no reaction takes place, indicate why. Pay attention to stereochemistry. NaCN DMF Br σ Ilm... Br H Br H H NaCN CH3OH KOtBu tBuOH NaBr H₂O LDA Et2O (CH3)2CHOH KCN DMSO NaOH H₂O, A LDA LDA Systemarrow_forwardQ7: For the following reactions, indicate the reaction conditions that would provide the indicated product in a high yield. Note the major reaction pathway that would take place (SN1, SN2, E1, or E2) Note: There may be other products that are not shown. There maybe more than one plausible pathway. Br H3C OH H3C CI ... H3C SCH2CH3 CI i SCH2CH3 ཨ་ Br System Settarrow_forwardQ2: Rank the compounds in each of the following groups in order of decreasing rate of solvolysis in aqueous acetone. OSO2CF3 OSO2CH3 OH a. b. CI Brarrow_forward
- ох 4-tert-butyl oxy cyclohex-1-ene Incorrect, 1 attempt remaining The systematic name of this compound classifies the -OR group as a substituent of the hydrocarbon, which is considered the principal functional group. The ether substituent is named with the suffix 'oxy'. The general format for the systematic name of a hydrocarbon is: [prefix/substituent] + [parent] + [functional group suffix] Substituents are listed in alphabetical order. Molecules with a chiral center will indicate the absolute configuration at the beginning of its name with the R and S notation.arrow_forward5. Compressibility (6 points total). The isothermal compressibility is a measure of how hard/easy it is to compress an object (how squishy is it?) at constant temperature. It is др defined as Br=-()=-(200²)T' (a) You might wonder why there is a negative sign in this formula. What does it mean when this quantity is positive and what does it mean when this quantity is negative? (b) Derive the formula for the isothermal compressibility of an ideal gas (it is very simple!) (c) Explain under what conditions for the ideal gas the compressibility is higher or lower, and why that makes sense.arrow_forward19. (3 pts) in Chapter 7 we will see a reaction of halocyclohexanes that requires that the halogen occupy an axial position with this in mind, would you expect cis-1-bromo-3-methylcyclohexane or trans-1-bromo-3-methylcyclohexane to be more reactive in this reaction? Briefly explain your choice using structures to support your answer. Mere-eries-cecleone) The tran-i-browse-3-methylcyclohexionearrow_forward
- Please help me calculate the undiluted samples ppm concentration. My calculations were 280.11 ppm. Please see if I did my math correctly using the following standard curve. Link: https://mnscu-my.sharepoint.com/:x:/g/personal/vi2163ss_go_minnstate_edu/EVSJL_W0qrxMkUjK2J3xMUEBHDu0UM1vPKQ-bc9HTcYXDQ?e=hVuPC4arrow_forwardProvide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H₁₂C C(CH3)3 C=C H3C CH3 CH3CH2CH CI CH3 Submit Answer Retry Entire Group 2 more group attempts remaining Previous Nextarrow_forwardArrange the following compounds / ions in increasing nucleophilicity (least to most nucleophilic) CH3NH2 CH3C=C: CH3COO 1 2 3 5 Multiple Choice 1 point 1, 2, 3 2, 1, 3 3, 1, 2 2, 3, 1 The other answers are not correct 0000arrow_forward
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning




