Chemical reactions

From WikiLectures

Chemical reactions are events in which substances of a different composition (products) are formed from starting substances (reactants); chemical reactions are described by a chemical equation.

  • reactants = starting substances entering a chemical reaction
  • products = newly formed substances arising from a chemical reaction

Basic chemical laws[edit | edit source]

  1. Law of conservation of mass – the mass of all reactants equals the mass of all products
  2. Law of conservation of energy – the energy of an isolated system is constant during a chemical reaction
  3. The law of constant combining ratios – the ratio of elements or parts of a given compound is always the same, it does not depend on the method of preparation of compounds

Types of reactions[edit | edit source]

  1.  Direct – creation of products
  2.  Reverse – reaction of products to form starting substances
  3.  Reversible – direct and reverse reactions take place mutually

Types of reactions according to external changes during the reaction[edit | edit source]

Synthesis[edit | edit source]

  • combination reaction
  • a reaction in which simpler starting substances combine to form more complex substances, e.g. N2 + 3 H2 → 2 NH3

Analysis[edit | edit source]

  • decomposition reaction
  • a reaction in which more complex substances are split into simpler substances, e.g. CaCO3 → CaO + CO2

Single-Replacement Reactions[edit | edit source]

  • substitution reaction
  • a reaction in which one reactant replaces an atom or functional group from another reactant (compound), e.g. 2 KI + Cl2 → 2 KCl + I2 (chlorine replaced iodine from potassium iodide)

Double-Replacement Reactions[edit | edit source]

  • conversion
  • is formed by the combination of two displacement (substitution) reactions, e.g. NaCl + H2SO4 → NaHSO4 + HCl

Types of reactions according to the reaction mechanism[edit | edit source]

Addition[edit | edit source]

  • A reaction in which molecules of another substance (e.g. water, hydrogen halides) are added to an organic compound bearing a multiple bond and the multiple bond disappears, e.g. CH2=CH2 + Cl2 → CH2 Cl-CH2 Cl
    • Electrophilic addition – an electrophilic reagent (a reagent with an electrophilic deficit) reacts with the π-electrons of multiple bonds, e.g. addition of hydrogen halides and halogens to alkenes or alkynes
    • Nucleophilic addition – a nucleophilic reagent (contains a non-bonding electron pair) is added to the carbon in the bond carrying a partial positive charge, the reaction is typical for carbonyl compounds

Elimination[edit | edit source]

  • A reaction in which a simple inorganic compound is split off and a multiple bond is simultaneously formed, e.g. CH3-CH2Cl → CH2=CH2 + HCl
    • Dehydration – water molecules are split off
    • Dehydrogenation – hydrogen molecules are split off
    • Dehydrohalogenation – hydrogen halide molecules are split off

Substitution[edit | edit source]

  • A reaction in which an atom or group of atoms is exchanged for another atom or group of atoms, the multiplicity of the bonds does not change
    • Radical substitution – characteristic of compounds with non-polar covalent bonds (e.g. alkanes), homolytic cleavage of bonds occurs and radicals are formed (very reactive particles with unpaired electron) reacting with the radical of the substituted atom, e.g. chlorination of hydrocarbons
    • Electrophilic substitution – a typical reaction of aromatic hydrocarbons in which they react with an electrophilic agent that is formed during the reaction, e.g. nitration of arenes (the nitro group NO2 in the form of a nitronium cation is introduced into the arene molecule)
    • Nucleophilic substitution – a nucleophilic reagent reacts with a carbon atom and a partially positive charge, the reaction is typical for alkyl halides

Permutation[edit | edit source]

  • Isomerization reaction in which the atoms inside the molecule are rearranged


Types of reactions according to the number of phases[edit | edit source]

Homogeneous[edit | edit source]

  • Reactions in which the reactants are in one phase, most often gaseous or liquid, e.g. H2 (g) + I2 (g) → 2 HI (g)

Heterogeneous[edit | edit source]

  • Reactions in which the reactants are in different phases and the reaction takes place at their phase interface, e.g. 2 HCl (aq) + Zn (s) → ZnCl2 (aq) + H2 (g)

Types of reactions according to the type of transferred particles[edit | edit source]

Oxidation-reduction[edit | edit source]

  • redox
  • reactions in which electrons are transferred between reaction components, taking place as two partial reactions - oxidation and reduction; certain atoms give up electrons, thereby becoming oxidized, and at the same time other atoms receive electrons, thereby reducing

Acid-base[edit | edit source]

  • protolytic
  • reactions in which the cation H+ is transferred ; substances that donate H+ cations are called acids, substances that accept H+ cations are called bases (according to the Brönsted-Lowry theory of acids and bases)

Coordination[edit | edit source]

  • complex forming
  • reactions during which whole groups of atoms are transferred and complex compounds are formed

Types of reactions according to the method of bond cleavage[edit | edit source]

Homolytic[edit | edit source]

  • reactions in which the covalent bond formed by atoms with the same (or almost the same) electronegativity splits symmetrically so that each of the resulting particles retains one electron and forms radicals, e.g. Cl – Cl → Cl ∙ + Cl ∙

Heterolytic[edit | edit source]

  • the opposite of homolysis
  • the bond splits asymmetrically, the bound particles have a large electronegativity difference, the more electronegative particle retains the entire electron pair from the bond and ions are formed, e.g. HCl → H+ + Cl-

Links[edit | edit source]

Related articles[edit | edit source]

Literature[edit | edit source]

  • SLEZINA, Miroslav. Biochemie pro studující medicíny. 2. edition. Karolinum, 2009. 0 pp. ISBN 978-80-246-1414-4.


  • BENEŠOVÁ, Marika – SATRAPOVÁ, Hana. Odmaturuj! z chemie. 1. edition. Didaktis, 0000. 0 pp. ISBN 80-862-8556-1.