Concept explainers
(a)
Interpretation:
The structural formula for a compound with molecular formula
Concept introduction:
The systematic naming of organic compound is given by
Rules for writing IUPAC name from structural formula are:
• First identify the longest carbon chain.
• The next step is to identify the groups attached to the longest chain.
• Identify the position, location, and number of the substituents bonded to the carbon chain.
• Use prefix di, tri, tetra if same type of substituents are present.
• Name the substituents in alphabetical order.
(b)
Interpretation:
The structural formula for a compound with molecular formula
Concept introduction:
The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.
Rules for writing IUPAC name from structural formula are:
• First identify the longest carbon chain.
• The next step is to identify the groups attached to the longest chain.
• Identify the position, location, and number of the substituents bonded to the carbon chain.
• Use prefix di, tri, tetra if same type of substituents are present.
• Name the substituents in alphabetical order.
(c)
Interpretation:
The structural formula for a compound with molecular formula
Concept introduction:
The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.
Rules for writing IUPAC name from structural formula are:
• First identify the longest carbon chain.
• The next step is to identify the groups attached to the longest chain.
• Identify the position, location, and number of the substituents bonded to the carbon chain.
• Use prefix di, tri, tetra if same type of substituents are present.
• Name the substituents in alphabetical order.
Trending nowThis is a popular solution!
Chapter 12 Solutions
Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version
- What is the difference in bonding and in general molecular formula between an alkene and a cycloalkane with the same number of carbon atoms?arrow_forwardWhat is the difference in bonding and in the general molecular formula between an alkene and an alkane with the same number of carbon atoms?arrow_forwardWhat are aromatic hydrocarbons? Benzene exhibits resonance. Explain. What are the bond angles in benzene? Give a detailed description of the bonding in benzene. The electrons in benzene are delocalized, while the electrons in simple alkenes and alkynes are localized. Explain the difference.arrow_forward
- 2. a) Explain what structural feature of the double bond is required for an alkene to exhibit cis-trans (geometric) isomerism? b) Which of the following alkenes can exhibit cis-trans isomerism? If the molecule exhibits cis- trans isomerism, draw and name the associated isomer. 1- pentene CH2=CHCH2CH2CH3 i) ii) 2- pentene CH3CH=CHCH₂CH3 -0arrow_forwardWrite Lewis structures and IUPAC names for the alkyne isomers of C4H6.arrow_forwardwrite the structure formulas of alkanes with molecular formula C6H14, which with chlorine give: a) three monochlorinated isomers? b) five monochlorinated isomers c) only two monochlorinated isomersarrow_forward
- A saturated acyclic hydrocarbon has the molecular formula of CxH₂x2. A hydrocarbon can be classified as unsaturated if it has fewer hydrogens than a saturated formula would predict. Classify the following hydrocarbon skeletal structure as saturated or unsaturated. A) saturated B) unsaturatedarrow_forwarddraw structural formulas for all isomeric alkanes with molecular formula C7H16. Predict which isomer has the lowest boiling point and which has the highest boiling point.arrow_forwardWrite the structure of the compound that will be produced in the following reaction? CH3 –C ≡ C–CH2– CH2 – CH3 + 2HBr→ a) Other than the combustion of alkanes, why are alkanes not reactive, or when they do react, they do so very slowly? B) What chemical reaction can alkenes and alkynes undergo that alkanes cannot? Explainarrow_forward
- 8. a) C3H$C1 has several structural isomers containing an alkene functional group. Complete the table by stating the systematic names and drawing the structural formulae of THREE structural isomers of C3H$Cl. Systematic Name Structural Formula b) A chemical test can be performed quickly in a school laboratory to distinguish between cyclohexanol and 1-methylcyclohexanol. Identify the reagent used in this test and describe the expected observations.arrow_forward6. Which of the following is not a homologous family of unsaturated hydrocarbons? a) Alkanesarrow_forwardDraw a skeletal (line-bond) structure of cyclohexane.arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning