Concept explainers
Videos
(a)
Interpretation:
The condensed structural formula has to be drawn for the given compounds without parentheses.
Concept Introduction:
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
In condensed structural formula for
The condensed structural formula for branched chain alkane can be entered using parentheses to give a linear (straight-line) condensed structural formula. Groups in parentheses are understood that it is attached to the carbon atom that precedes the group.
(b)
Interpretation:
The condensed structural formula has to be drawn for the given compounds without parentheses.
Concept Introduction:
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
In condensed structural formula for alkanes, the repeating
The condensed structural formula for branched chain alkane can be entered using parentheses to give a linear (straight-line) condensed structural formula. Groups in parentheses are understood that it is attached to the carbon atom that precedes the group.
(c)
Interpretation:
The condensed structural formula has to be drawn for the given compounds without parentheses.
Concept Introduction:
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
In condensed structural formula for alkanes, the repeating
The condensed structural formula for branched chain alkane can be entered using parentheses to give a linear (straight-line) condensed structural formula. Groups in parentheses are understood that it is attached to the carbon atom that precedes the group.
(d)
Interpretation:
The condensed structural formula has to be drawn for the given compounds without parentheses.
Concept Introduction:
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
In condensed structural formula for alkanes, the repeating
The condensed structural formula for branched chain alkane can be entered using parentheses to give a linear (straight-line) condensed structural formula. Groups in parentheses are understood that it is attached to the carbon atom that precedes the group.
Want to see the full answer?
Check out a sample textbook solution
Chapter 1 Solutions
Organic And Biological Chemistry
- How does the structure of a cycloalkane differ from that of a straight-chain or branched-chain alkane?arrow_forwardWhat is the name of the compound with the formula CH3C(CH3)2CH2CH(CH3)CH3,which is one of the substances found in gasoline A. Octane B.2,4-dimethylpentane C.2,2,4-methylpentane D.2,2,4-trimethylpentane E. 2,4,4-methylpentanearrow_forwardCH2-CH2-CH3 Type of functional group r. CH2-CH2-CH3 Common Name Type of functional group H3C-C-o IUPAC H3C- Common Name H,C-CH,-CH,-CH,-CH,-NH-ċ-CH -CH3 t. Type of functional grouparrow_forward
- ISOMERISMarrow_forward1. Name and draw the isomers form from the given molecular formula. a. C₂H16 b. C4H,Br₂ 2. Draw the structure of each of the following cycloalkanes a. 1-Bromo-2-methylcyclobutane b. 1,2-Dibromo-3-methylcyclohexanearrow_forward4. Which of the following has isomeric forms?a. C2H3Clb. C2H5Clc. C2HCld. C2H4Cl2 5. Which of the following hydrocarbons always gives the same product when one of its hydrogen atoms is replaced by a chlorine atom.a. Hexaneb. Hex-1-enec. Cyclohexaned. Cyclohexenearrow_forward
- Classify the following hydrocarbons as alkanes, cycloalkane, alkene, cycloalkenes, alkyne, cycloalkyne, or aromatic.a. CH2 CH CH2b. CH3 C (CH3)2 CH (CH2CH3) CH2 CH2 CH (CH3)2c. (CH3)3 C C C CH (CH3) CH2 CH3arrow_forward1. Using the grignard reaction of alkanes what is the resulting alkane if the reactant is C4H9Br? a. ethane b. propane c. butane d. pentane 2. Using the grignard reaction of alkanes what is the resulting alkane if the reactant is C5H11F? a. ethane b. propane c. butane d. pentane 3. Using Cl2 in C2H4Cl2 will result in HCl and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. not posiblearrow_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
- Constitutional isomers are compounds which have the same molecular formula but different structural formulae. They are different compounds with different physical and chemical properties.a. Rearrange your model of n-hexane to make as many possible isomers of C6H14 as you can. Draw the structural formula and write down the IUPAC name for each isomer that you make.b. Constitutional isomers can also have different functional groups. Make all possible isomers of C3H8O. Write down the structural formulae and IUPAC names for all the compounds you make. Hint: Consider alcohol and ether functional groups.arrow_forwardWhich structures have the correct IUPAC names? * CH3 CH3 Br Br I. 2-bromotoluene II. para methyl, meta chloro bromobenzene NO2 OCH3 `C. ĊH-CH3 III. meta chloroaniline IV. para ethylanisole O III,IV 1,IV O II, IIarrow_forwardThe addition of four identical monomer molecules produces the naturally occurring molecule shown below. H₂C H₂C H₂C CH CH₂ CH₂ CH₂ HC CH₂ CH₂ CH₂ CH₂ CH₂ CH What could be the structural formula of the monomer? A. CH2=C(CH3)CH2CH3 B. CH3CH=CHCH=CH₂ C. CH3CH₂CH₂CH=CH2 D. CH2=C(CH3)CH=CH2 CH,arrow_forward
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning