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Chapter 11: Introduction to Organic Chemistry: Hydrocarbons

11.1: Organic Compounds

  • Organic Chemistry: The study of carbon compounds.

  • Organic Compounds: Always contain carbon and hydrogen, and sometimes other nonmetals such as oxygen, sulfur, nitrogen, phosphorus, or a halogen.

  • Hydrocarbon: These organic compounds consist of only carbon and hydrogen.

    • A hydrocarbon is referred to as a saturated hydrocarbon when all the bonds in the molecule are single bonds.


11.2: Alkanes

  • Alkanes: These are a type of hydrocarbon in which the carbon atoms are connected only by single bonds

  • Names of alkanes end in –ane.

    • Methane, Ethane, Propane, Butane, etc.

  • IUPAC system: A system for naming organic compounds devised by the International Union of Pure and Applied Chemistry.

  • Alkanes with five or more carbon atoms in a chain are named using Greek prefixes:

    • pent, hex, hept, oct, non, and dec.

Condensed Structural Formulas

  • Each carbon atom and its attached hydrogen atoms are written as a group. A subscript indicates the number of hydrogen atoms bonded to each carbon atom.

Condensed Structural Formula

  • Molecular formula: It gives the total number of carbon and hydrogen atoms, but does not indicate their arrangement in the molecule.

  • Skeletal Formula: A simplified structure that shows the carbon skeleton in which carbon atoms are represented at the end of each line or as corners.

Conformations of Alkanes

  • Because an alkane has only single carbon–carbon bonds, the groups attached to each C are not in fixed positions.

  • They can rotate freely about the bond connecting the carbon atoms. This motion is analogous to the independent rotation of the wheels of a toy car

  • Conformations: The different arrangements that occur during the rotation of a single bond.

  • Cycloalkanes: Hydrocarbons can also form cyclic or ring structures, which have two fewer hydrogen atoms than the corresponding alkanes.

    • Cyclopropane: The simplest cycloalkane that has a ring of three carbon atoms bonded to six hydrogen atoms.


11.3: Alkanes with Substituents

  • Substituent

    • When an alkane has four or more carbon atoms, the atoms can be arranged here, which is attached to the carbon chain.

    • Branched Alkane: An alkane with at least one branch.

    • Structural Isomers: When the two compounds have the same molecular formula but different arrangements of atoms.

  • Substituents in Alkanes

    • Alkyl Group: An alkane that is missing one hydrogen atom.

    • The alkyl group is named by replacing the –ane ending of the corresponding alkane name with –yl.

    • When a halogen atom is attached to a carbon chain, it is named as a halo group: fluoro, chloro, bromo, or iodo.

  • Haloalkanes: Halogen atoms replace hydrogen atoms in an alkane.


11.4: Properties of Alkanes

  • The first four alkanes — methane, ethane, propane, and butane — are gases at room temperature and are widely used as heating fuels.

  • Alkanes having five to eight carbon atoms are liquids at room temperature; they are highly volatile.

  • Liquid alkanes with 9 to 17 carbon atoms have higher boiling points and are found in kerosene, diesel, and jet fuels.

    • Motor oil: A mixture of high-molecular-weight liquid hydrocarbons and is used to lubricate the internal components of engines.

    • Mineral oil: A mixture of liquid hydrocarbons and is used as a laxative and a lubricant.

  • Alkanes with 18 or more carbon atoms are waxy solids at room temperature.

    • Paraffins: They are used in waxy coatings added to fruits and vegetables to retain moisture, inhibit mold, and enhance appearance.

  • Petroleum: A semisolid mixture of hydrocarbons with more than 25 carbon atoms used in ointments and cosmetics and as a lubricant.

  • Alkanes are nonpolar, which makes them insoluble in water.

    • However, they are soluble in nonpolar solvents such as other alkanes.

  • The carbon–carbon single bonds in alkanes are difficult to break, which makes them the least reactive family of organic compounds.


11.5: Alkenes and Alkynes

  • Alkenes and alkynes are families of hydrocarbons that contain double and triple bonds.

    • They are unsaturated hydrocarbons because they do not contain the maximum number of hydrogen atoms, as do alkanes.

    • They react with hydrogen gas to increase the number of hydrogen atoms to become alkanes, which are saturated hydrocarbons.

  • Alkenes: These contain one or more carbon–carbon double bonds that form when adjacent carbon atoms share two pairs of valence electrons.

  • Alkyne: A triple bond forms when two carbon atoms share three pairs of valence electrons.

  • The IUPAC names for alkenes and alkynes are similar to those of alkanes.

    • Using the alkane name with the same number of carbon atoms, the –ane ending is replaced with –ene for an alkene and –yne for an alkyne.

  • Cycloalkenes: These are some alkenes that have a double bond within a ring structure.


11.6: Cis–Trans Isomers

  • Cis–Trans Isomers: These are compounds that have different configurations because of the presence of a rigid structure in their molecule.

  • Cis Isomer: An isomer of an alkene in which similar groups in the double bond are on the same side.

  • Trans Isomer: An isomer of an alkene in which similar groups in the double bond are on opposite sides.


11.7: Additional Reactions

  • The most characteristic reaction of alkenes is the addition of atoms or groups of atoms to the carbon atoms in a double bond.

    • It occurs because double bonds are easily broken, providing electrons to form new single bonds.

  • Hydrogenation

    • H atoms add to each of the carbon atoms in a double bond of an alkene.

    • The double bonds are converted to single bonds in alkanes.

    • A catalyst is used to speed up the reaction.

  • Hydration

    • An alkene reacts with water (H — OH).

    • A hydrogen atom (H —) from water forms a bond with one carbon atom in the double bond, and the oxygen atom in —OH forms a bond with the other carbon.

    • The reaction is catalyzed by a strong acid such as H2SO4.


11.8: Aromatic Compounds

  • In 1825, Michael Faraday isolated a hydrocarbon called benzene, which had the molecular formula C6H6.

  • A molecule of benzene consists of a ring of six carbon atoms with one hydrogen atom attached to each carbon.

  • Aromatic Compounds: Family of benzene compounds.

  • In 1865, August Kekulé proposed that the carbon atoms in benzene were arranged in a flat ring with alternating single and double bonds between the carbon atoms.

MA

Chapter 11: Introduction to Organic Chemistry: Hydrocarbons

11.1: Organic Compounds

  • Organic Chemistry: The study of carbon compounds.

  • Organic Compounds: Always contain carbon and hydrogen, and sometimes other nonmetals such as oxygen, sulfur, nitrogen, phosphorus, or a halogen.

  • Hydrocarbon: These organic compounds consist of only carbon and hydrogen.

    • A hydrocarbon is referred to as a saturated hydrocarbon when all the bonds in the molecule are single bonds.


11.2: Alkanes

  • Alkanes: These are a type of hydrocarbon in which the carbon atoms are connected only by single bonds

  • Names of alkanes end in –ane.

    • Methane, Ethane, Propane, Butane, etc.

  • IUPAC system: A system for naming organic compounds devised by the International Union of Pure and Applied Chemistry.

  • Alkanes with five or more carbon atoms in a chain are named using Greek prefixes:

    • pent, hex, hept, oct, non, and dec.

Condensed Structural Formulas

  • Each carbon atom and its attached hydrogen atoms are written as a group. A subscript indicates the number of hydrogen atoms bonded to each carbon atom.

Condensed Structural Formula

  • Molecular formula: It gives the total number of carbon and hydrogen atoms, but does not indicate their arrangement in the molecule.

  • Skeletal Formula: A simplified structure that shows the carbon skeleton in which carbon atoms are represented at the end of each line or as corners.

Conformations of Alkanes

  • Because an alkane has only single carbon–carbon bonds, the groups attached to each C are not in fixed positions.

  • They can rotate freely about the bond connecting the carbon atoms. This motion is analogous to the independent rotation of the wheels of a toy car

  • Conformations: The different arrangements that occur during the rotation of a single bond.

  • Cycloalkanes: Hydrocarbons can also form cyclic or ring structures, which have two fewer hydrogen atoms than the corresponding alkanes.

    • Cyclopropane: The simplest cycloalkane that has a ring of three carbon atoms bonded to six hydrogen atoms.


11.3: Alkanes with Substituents

  • Substituent

    • When an alkane has four or more carbon atoms, the atoms can be arranged here, which is attached to the carbon chain.

    • Branched Alkane: An alkane with at least one branch.

    • Structural Isomers: When the two compounds have the same molecular formula but different arrangements of atoms.

  • Substituents in Alkanes

    • Alkyl Group: An alkane that is missing one hydrogen atom.

    • The alkyl group is named by replacing the –ane ending of the corresponding alkane name with –yl.

    • When a halogen atom is attached to a carbon chain, it is named as a halo group: fluoro, chloro, bromo, or iodo.

  • Haloalkanes: Halogen atoms replace hydrogen atoms in an alkane.


11.4: Properties of Alkanes

  • The first four alkanes — methane, ethane, propane, and butane — are gases at room temperature and are widely used as heating fuels.

  • Alkanes having five to eight carbon atoms are liquids at room temperature; they are highly volatile.

  • Liquid alkanes with 9 to 17 carbon atoms have higher boiling points and are found in kerosene, diesel, and jet fuels.

    • Motor oil: A mixture of high-molecular-weight liquid hydrocarbons and is used to lubricate the internal components of engines.

    • Mineral oil: A mixture of liquid hydrocarbons and is used as a laxative and a lubricant.

  • Alkanes with 18 or more carbon atoms are waxy solids at room temperature.

    • Paraffins: They are used in waxy coatings added to fruits and vegetables to retain moisture, inhibit mold, and enhance appearance.

  • Petroleum: A semisolid mixture of hydrocarbons with more than 25 carbon atoms used in ointments and cosmetics and as a lubricant.

  • Alkanes are nonpolar, which makes them insoluble in water.

    • However, they are soluble in nonpolar solvents such as other alkanes.

  • The carbon–carbon single bonds in alkanes are difficult to break, which makes them the least reactive family of organic compounds.


11.5: Alkenes and Alkynes

  • Alkenes and alkynes are families of hydrocarbons that contain double and triple bonds.

    • They are unsaturated hydrocarbons because they do not contain the maximum number of hydrogen atoms, as do alkanes.

    • They react with hydrogen gas to increase the number of hydrogen atoms to become alkanes, which are saturated hydrocarbons.

  • Alkenes: These contain one or more carbon–carbon double bonds that form when adjacent carbon atoms share two pairs of valence electrons.

  • Alkyne: A triple bond forms when two carbon atoms share three pairs of valence electrons.

  • The IUPAC names for alkenes and alkynes are similar to those of alkanes.

    • Using the alkane name with the same number of carbon atoms, the –ane ending is replaced with –ene for an alkene and –yne for an alkyne.

  • Cycloalkenes: These are some alkenes that have a double bond within a ring structure.


11.6: Cis–Trans Isomers

  • Cis–Trans Isomers: These are compounds that have different configurations because of the presence of a rigid structure in their molecule.

  • Cis Isomer: An isomer of an alkene in which similar groups in the double bond are on the same side.

  • Trans Isomer: An isomer of an alkene in which similar groups in the double bond are on opposite sides.


11.7: Additional Reactions

  • The most characteristic reaction of alkenes is the addition of atoms or groups of atoms to the carbon atoms in a double bond.

    • It occurs because double bonds are easily broken, providing electrons to form new single bonds.

  • Hydrogenation

    • H atoms add to each of the carbon atoms in a double bond of an alkene.

    • The double bonds are converted to single bonds in alkanes.

    • A catalyst is used to speed up the reaction.

  • Hydration

    • An alkene reacts with water (H — OH).

    • A hydrogen atom (H —) from water forms a bond with one carbon atom in the double bond, and the oxygen atom in —OH forms a bond with the other carbon.

    • The reaction is catalyzed by a strong acid such as H2SO4.


11.8: Aromatic Compounds

  • In 1825, Michael Faraday isolated a hydrocarbon called benzene, which had the molecular formula C6H6.

  • A molecule of benzene consists of a ring of six carbon atoms with one hydrogen atom attached to each carbon.

  • Aromatic Compounds: Family of benzene compounds.

  • In 1865, August Kekulé proposed that the carbon atoms in benzene were arranged in a flat ring with alternating single and double bonds between the carbon atoms.