- •Unit I organic chemistry
- •Functional groups
- •Physical properties of an organic substance
- •Organic Compounds
- •Revision exercises
- •Unit II types of chemical reactions
- •Basic concepts of chemical reactions
- •Classification by types of reactants
- •Classification by reaction mechanism
- •Revision exercises
- •Unit III types of bonds
- •Ionic Bonds
- •Covalent Bonds
- •Metallic and Hydrogen Bonds
- •Revision exercises
- •Unit IV Isomerism
- •The Isomerism tree
- •Revision exercises
- •History of isomerism
- •Unit V Hydrocarbons
- •Hydrocarbons Classification
- •Revision exercises
- •Unit VI alkanes, alkenes, alkynes Alkanes
- •Alkenes
- •Alkynes
- •Revision exercises
- •Unit VII halogens
- •Elements
- •Applications of Halogens
- •Halogen derivatives
- •Revision exercises
- •Unit VIII nitro compounds
- •Physical properties of nitro compounds
- •The physical properties of amines
- •Various methods of organic synthesis of nitro compounds
- •Revision exercises
- •Unit IX Alcohols
- •Physical Properties of Alcohols
- •Chemical Properties of Alcohols
- •Preparation of Alcohols
- •Revision exercises
- •Nomenclature
- •Unit X Phenols
- •Natural sources of phenols
- •Revision exercises
- •Nomenclature of phenols
- •Unit XI ethers
- •Ether usage
- •Revision exercises
- •Unit XII aldehydes and ketones
- •Important aldehydes and ketones
- •Properties of aldehydes and ketones
- •Revision exercises
- •Unit XIII сarboxylic acid
- •Properties of carboxylic acids
- •Classes of carboxylic acids
- •Synthesis of carboxylic acids
- •Revision exercises
- •Unit XIV esters
- •Revision exercises
- •Unit XV carbohydrates
- •Carbohydrate benefits
- •Revision exercises
- •Unit XVI Fats
- •Fats and Oils
- •Saturated and Unsaturated Fatty Acids
- •Measures of Unsaturation
- •Revision exercises
- •Unsaturated Fatty Acids
- •Unit XVII proteins and peptides
- •Physicochemical properties of proteins
- •Classification by biological functions
- •Revision exercises
- •Unit XVIII Catalysts and Reaction Conditions Chemical reactions and catalysts
- •Enzymes
- •Revision exercises
- •Catalysts and Catalysis
- •Unit XIX bioactive compounds and biochemistry
- •Hormones
- •Major Types of Hormones
- •Vitamins
- •Biochemistry
- •Methods in biochemistry
- •Revision exercises
- •How to read chemical reactions
Classification by types of reactants
Oxidation-reduction reactions. Oxidation-reduction (redox) reactions involve the transfer of one or more electrons from a reducing agent to an oxidizing agent. This has the effect of reducing the real or apparent electric charge on an atom in the substance being reduced and of increasing the real or apparent electric charge on an atom in the substance being oxidized. Carbon atoms may have any oxidation state from –4 (e.g. CH4 ) to +4 (e.g. CO2 ), depending upon their substituents. Fortunately, we need not determine the absolute oxidation state of each carbon atom in a molecule, but only the change in oxidation state of those carbons involved in a chemical transformation. To determine whether a carbon atom has undergone a redox change during a reaction we simply note any changes in the number of bonds to hydrogen and the number of bonds to more electronegative atoms that has occurred. Bonds to other carbon atoms are ignored.
Simple redox reactions include the reactions of an element with oxygen. For example, magnesium burns in oxygen to form magnesium oxide (MgO). Redox reactions are the source of the energy of batteries. The electric current generated by a battery arises because electrons are transferred from a reducing agent to an oxidizing agent through the external circuitry.
Acid-base reactions. Acids and bases are important compounds in the natural world, so their chemistry is central to any discussion of chemical reactions. First, acid-base reactions are among the simplest to recognize and understand. Second, some classes of organic compounds have distinctly acidic properties, and some other classes behave as bases, so we need to identify these aspects of their chemistry. Finally, many organic reactions are catalyzed by acids and/or bases. Organic chemists use two acid-base theories for interpreting and planning their work: the Brønsted-Lowry theory and the Lewis theory.
Classification by reaction result
Decomposition reactions. Decomposition reactions are processes in which chemical species break up into simpler parts. Usually, decomposition reactions require energy input. For example, a common method of producing oxygen gas in the laboratory is the decomposition of potassium chlorate (KClO3) by heat.
Another decomposition reaction is the production of sodium (Na) and chlorine (Cl2) by electrolysis of molten sodium chloride (NaCl) at high temperature.
A decomposition reaction that was very important in the history of chemistry is the decomposition of mercury oxide (HgO) with heat to give mercury metal (Hg) and oxygen gas. This is the reaction used by 18th-century chemists Carl Wilhelm Scheele, Joseph Priestley, and Antoine-Laurent Lavoisier in their experiments on oxygen.
Substitution, elimination and addition reactions. These terms are particularly useful in describing organic reactions. In a substitution reaction, an atom or group of atoms in a molecule is replaced by another atom or group of atoms. For example, methane (CH4) reacts with chlorine (Cl2) to produce chloromethane (CH3Cl), a compound used as a topical anesthetic. In this reaction, a chlorine atom is substituted for a hydrogen atom. Substitution reactions are widely used in industrial chemistry. For example, substituting two of the chlorine atoms on chloroform (CHCl3) with fluorine atoms produces chlorodifluoromethane (CHClF2). This product undergoes a further reaction when heated strongly.
2CHClF2(g) → F2C=CF2(g) + 2HCl(g)
This latter reaction is an example of an elimination reaction, a hydrogen atom and a chlorine atom being eliminated from the starting material as hydrochloric acid (HCl). The other product is tetrafluoroethylene, a precursor to the polymer known commercially as Teflon. Addition reactions are the opposite of elimination reactions. As the name implies, one molecule is added to another. An example is the common industrial preparation of ethanol (CH3CH2OH). Historically, this compound was made by fermentation. However, since the early 1970s, it has also been made commercially by the addition of water to ethylene.
C2H4+ H2O → CH3CH2OH
Polymerization reactions. Polymers are high-molecular-weight compounds, formed by the aggregation of many smaller molecules called monomers. The plastics that have so changed society and the natural and synthetic fibres used in clothing are polymers. There are two basic ways to form polymers: (a) linking small molecules together, a type of addition reaction, and (b) combining two molecules (of the same or different type) with the elimination of a stable small molecule such as water. This latter type of polymerization combines addition and elimination reactions and is called a condensation reaction.
An example of the first type of reaction is the union of thousands of ethylene molecules that gives polyethylene. Other addition polymers include polypropylene (made by polymerizing H2C=CHCH3), polystyrene(from H2C=CH C6H5), and polyvinyl chloride (from H2C=CHCl).
Starch and cellulose are examples of the second type of polymer. These are members of a class of compounds called carbohydrates, substances with formulas that are multiples of the simple formula CH2O. Both starch and cellulose are polymers of glucose, a sugar with the formula C6H12O6. In both starch and cellulose, molecules of glucose are joined together with concomitant elimination of a molecule of water for every linkage formed.
Solvolysis and hydrolysis. A solvolysis reaction is one in which the solvent is also a reactant. Solvolysis reactions are generally named after the specific solvent. The term hydrolysis is used when water is involved. If a compound is represented by the formula AB (in which A and B are atoms or groups of atoms) and water is represented by the formula HOH, the hydrolysis reaction may be represented by the reversible chemical reaction
AB + HOH ⇌ AH + BOH
Hydrolysis of an organic compound is illustrated by the reaction of water with esters. The hydrolysis of an ester produces an acid and an alcohol.
Hydrolysis reactions play an important role in chemical processes that occur in living organisms. Proteins are hydrolyzed to amino acids, fats to fatty acids and glycerol, and starches and complex sugars to simple sugars. In most instances, the rates of these processes are enhanced by the presence of enzymes, biological catalysts. Hydrolysis reactions are also important to acid-base behaviour. Hydrolysis reactions account for the basic character of many common substances.
