Tertiary alcohols do not undergo oxidation under these conditions and remain unchanged.
Nomenclature of alkanes: Determine the longest continuous chain as the parent hydrocarbon.
Cycloalkanes: Determine the parent alkane name, with the ring being the parent hydrocarbon unless a longer alkyl substituent is present, and naming format: cyclo(#)ane (e.g., cyclohexane, cyclopentane).
If the functional group gets the same number from both directions, use the direction that gives the substituent the lower number.
Normal or straight-chain alkanes form a homologous series, involving compounds differing by an additional –CH2– unit.
Isomers have identical formulas but differ in properties and atom arrangement.
Butane (C4H10) is produced by removing a hydrogen from propane and adding -CH3.
Alkanes are characterized by being odorless compounds.
Normal alkanes with 1 to 4 carbon atoms are gases, while those with 5 to 20 carbon atoms are liquids.
Properties within a homologous series are closely related and vary systematically.
Substituents on nitrogen are indicated with italicized N-.
Methane is the simplest alkane with one carbon atom.
Alkanes are saturated hydrocarbons, with single bonds, no double or triple bonds.
Alkanes lack functional groups, making them less abundant in the human body.
Substituting an end carbon of propane with -CH3 yields a linear butane (CH3–CH3–CH3–CH3), while substituting the central carbon of propane yields a branched butane.
Normal alkanes have all carbon atoms form a continuous chain, while branched alkanes have at least one carbon atom not part of a continuous chain.
Boiling points of normal alkanes increase smoothly with the length of the carbon chain, with increasing dispersion forces contributing to this pattern.
Hydrocarbons are the simplest organic compounds, containing only carbon and hydrogen.
The general formula for alkanes is CnH2n+2, where 'n' represents the number of carbon atoms.
For multiple substituents, cite them in alphabetical order.
Hydrogen atoms in propane are not geometrically equivalent, providing multiple substitution positions.
IUPAC nomenclature treats the halogen as a substituent, replacing "ine" in the halogen name with "o" (e.g., chloromethane, 1,1-dichloroethane).
Ethyne (C2H2), also known as Acetylene, is the simplest alkyne.
Benzene (C6H6), also known as Benzene, is the simplest aromatic hydrocarbon.
Liquid alkanes with higher molecular weight act as emollients (skin softeners) when applied to the skin.
Paraffin wax, derived from alkanes, is used in milk cartons and wax paper due to its inert nature.
Alkanes and hydrocarbons are less dense than water, so they float on it.
Mineral oil, an alkane mixture, can replace natural skin oils.
The insolubility in water of alkanes and hydrocarbons is due to their nonpolar nature.
The most significant reaction of alkanes is combustion, which releases large amounts of heat and is widely used for hydrocarbons as fuels.
Natural gas contains methane (80% to 95%), ethane, and trace amounts of other hydrocarbons.
Unsaturated hydrocarbons contain one or more double or triple bonds between carbon atoms and belong to three classes: alkenes, alkynes, and aromatic hydrocarbons.
Ethene (C2H4), also known as Ethylene, is the simplest alkene.
Those with more than 20 carbon atoms are waxy solids.
Petroleum jelly, a semisolid mixture of alkanes, serves as both an emollient and a protective film.
Hydrocarbons, including alkanes, are hydrophobic (insoluble in water) and the term "paraffins" is used synonymously with alkanes.
Incomplete combustion of hydrocarbons may result in the production of carbon monoxide (CO) or even solid carbon, which is undesirable as CO is toxic, and carbon deposits hinder engine performance.
Propane and butane are extracted from natural gas and packaged in pressurized metal containers.
Alkanes do not react with halogens like chlorine and bromine.
In the body's carbohydrate metabolism, fumaric acid undergoes hydration catalyzed by the enzyme fumarase.