Concept explainers
(a)
Interpretation:
Structural formula for the given halogenated hydrocarbon has to be drawn.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as
Structural formula for halogenated hydrocabons:
From the IUPAC name or common name that is given for the halogenated hydrocarbon, the structural formula can be drawn. The parent hydrocarbon is present in the end when considering IUPAC name and in common name, the parent hydrocarbon is present in the first part as an alkyl group.
(b)
Interpretation:
Structural formula for the given halogenated hydrocarbon has to be drawn.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
IUPAC nomenclature for halogenated alkanes/cycloalkanes:
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as alkyl halides. These are not IUPAC names. They are common names. In a common name, two parts are present. First part is the name of the hydrocarbon (alkyl group). Second part gives the halogen present in the compound. The halogen is considered as though it is present as an ion even though no ions are present.
Structural formula for halogenated hydrocabons:
From the IUPAC name or common name that is given for the halogenated hydrocarbon, the structural formula can be drawn. The parent hydrocarbon is present in the end when considering IUPAC name and in common name, the parent hydrocarbon is present in the first part as an alkyl group.
(c)
Interpretation:
Structural formula for the given halogenated hydrocarbon has to be drawn.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
IUPAC nomenclature for halogenated alkanes/cycloalkanes:
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as alkyl halides. These are not IUPAC names. They are common names. In a common name, two parts are present. First part is the name of the hydrocarbon (alkyl group). Second part gives the halogen present in the compound. The halogen is considered as though it is present as an ion even though no ions are present.
Structural formula for halogenated hydrocabons:
From the IUPAC name or common name that is given for the halogenated hydrocarbon, the structural formula can be drawn. The parent hydrocarbon is present in the end when considering IUPAC name and in common name, the parent hydrocarbon is present in the first part as an alkyl group.
(d)
Interpretation:
Structural formula for the given halogenated hydrocarbon has to be drawn.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
IUPAC nomenclature for halogenated alkanes/cycloalkanes:
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as alkyl halides. These are not IUPAC names. They are common names. In a common name, two parts are present. First part is the name of the hydrocarbon (alkyl group). Second part gives the halogen present in the compound. The halogen is considered as though it is present as an ion even though no ions are present.
Structural formula for halogenated hydrocabons:
From the IUPAC name or common name that is given for the halogenated hydrocarbon, the structural formula can be drawn. The parent hydrocarbon is present in the end when considering IUPAC name and in common name, the parent hydrocarbon is present in the first part as an alkyl group.
Want to see the full answer?
Check out a sample textbook solutionChapter 12 Solutions
Bundle: General, Organic, and Biological Chemistry, 7th + OWLv2 Quick Prep for General Chemistry, 4 terms (24 months) Printed Access Card
- What is natural gas? a. a gas that forms from decaying vegetation b. a mixture of hydrocarbon gases, mostly methane c. a gas that forms naturally from coal d. naturally occurring hydrogenarrow_forwardWhat is the product of a substitution reaction if the reactants are fluoroethane and sodium hydroxide? A. ethanol and sodium fluoride B. flouroethanol and sodium hydride C. ethane and sodium fluoridearrow_forward1. Which of the following fuel has the lowest heat of combustion?a.Methaneb.Octanec.Coald.Ethanol 2. What is the process of breaking larger hydrocarbon molecules into smaller ones at low temperature through the use of catalyst in order to obtain higher quality of gasoline?a.Thermal crackingb.Catalytic crackingc.Catalytic reformingd.Catalytic combination 3. What is the most common oxidizing agent available in the atmosphere that can be used to generate fire?a.hydrogen peroxideb.oxygenc.ozoned.nitrous oxidearrow_forward
- A. Amine B. Alkane C. Ester D. Ketone E. Alcohol F. Ether G. Aromatic Hydrocarbon H. Carboxylic Acid I. Amide J. Alkene K. Alkyne L. Alkyl Halidearrow_forwardName one structural isomer created by changing theposition of one or more halogen atoms in each alkylhalide.a. 2-chloropentane c. 1,3-dibromocyclopentaneb. 1,1-difluropropane d. 1-bromo-2-chloroethanearrow_forward1. Identify the SYSTEMATIC name of the aliphatic hydrocarbon a. 1-pentenyicyclopentane b. 1-cyclopentylpent-2-yne c. 1-pentenecyclopent-2-yne d. 1-pentenyicyclopentane 2. Identify the SYSTEMATIC name of the aliphatic hydrocarbon a. Trans-1,2-propylcyclopropane b. Trans-1,2-diisopropylcyclopropane c. Cis-1,2-propylcyclopropane d. Cis-1,2-diisopropylcyclopropane 3. Identify the SYSTEMATIC name of the aliphatic hydrocarbon 3,10-dimethyl-2-decacen-6-yne 3,10-dimethyl-2-dodocen-6-yne 3,10-dimethyl-10-decacen-6-yne d. 3,10-dimethyl-10-dodocen-6-yne a. b. C. 4. Identify which type of isomer the following structures represent HO a. Skeletal Isomer b. E/Z isomer c. Cis/Trans isomer OH OH d. Positional isomer 5. Identify which type of isomer the following structures represent a. Skeletal Isomer Br b. E/Z isomer c Cis/Trans isomer Br d. Positional isomerarrow_forward
- A hydrocarbon containing one or more -C=C- bonds. a. addition reaction b. aliphatic compound c. alkene d. alkyne e. aromatic hydrocarbon f. hydration g. hydrogenation h. monomer i. phenyl group j. polycyclic aromatic hydrocarbon k. polymerarrow_forwardWrite the condensed structural formula for the following organic compound. a. 3 methyl hexane b. 1, 2, 3 tri Flouro cyclohexene. c. 1,3,5 tricholoro cyclo hexane d. 3 ethyl-1-butyne e 2 ethyl - 1 - butenearrow_forwarda. Name the hydrocarbons in the reaction.b. Circle and identify the functional group in the hydrocarbons.arrow_forward
- Predict the functional group of the product for the following reaction. a. amide b. hemiacetal c. carboxylic acid d. acetal e. ester f. aldehyde g. alcoholarrow_forwardThe dehydration of an alcohol produces which organic functional group and steam? a. alkyne b. aldehyde c. alkene d. ketone e. carboxylic acid and an alcoholarrow_forward6. Any organic compound that contains a benzene ring or similar feature. O a. addition reaction Ob. aliphatic compound Oc. alkene d. alkyne Oe. aromatic hydrocarbon Of. hydration g. hydrogenation h. monomer Oi. phenyl group j. polycyclic aromatic hydrocarbon k. polymer I. unsaturated hydrocarbonarrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
- Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning