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===Addition===
===Addition===


*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. CH<sub>2</sub>=CH<sub>2</sub> + Cl<sub>2</sub> → CH<sub>2</sub> Cl-CH<sub>2</sub> Cl
*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. CH<sub>2</sub>=CH<sub>2</sub> + Cl<sub>2</sub> → CH<sub>2</sub> Cl-CH<sub>2</sub> Cl
**'''Electrophilic addition''' – an electrophilic reagent (a reagent with an electrophilic deficit) reacts with the [[Chemická vazba#Vazba P.C3.8D.CF.80|π-electrons]] of multiple bonds, e.g. addition of hydrogen halides and [[halogeny|halogens]] to alkenes or alkynes
**'''Electrophilic addition''' – an electrophilic reagent (a reagent with an electrophilic deficit) reacts with the [[Chemická vazba#Vazba P.C3.8D.CF.80|π-electrons]] of multiple bonds, e.g. addition of hydrogen halides and [[halogeny|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]]
**'''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]]
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===Elimination===
===Elimination===


*a reaction in which a simple inorganic compound is split off and a multiple bond is simultaneously formed, e.g.  CH<sub>3</sub>-CH<sub>2</sub>Cl → CH<sub>2</sub>=CH<sub>2</sub> + HCl
*A reaction in which a simple inorganic compound is split off and a multiple bond is simultaneously formed, e.g.  CH<sub>3</sub>-CH<sub>2</sub>Cl → CH<sub>2</sub>=CH<sub>2</sub> + HCl
**'''Dehydration''' – water molecules are split off
**'''Dehydration''' – water molecules are split off
**'''Dehydrogenation''' – hydrogen molecules are split off
**'''Dehydrogenation''' – hydrogen molecules are split off
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===Substitution===
===Substitution===


*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
*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''' – charakteristická pro sloučeniny s nepolárními kovalentními vazbami (např. alkany), dochází k homolytickému štěpení vazeb a vznikají radikály (velmi reaktivní částice s nepárovým elektronem) reagující s radikálem substituovaného atomu, např. chlorace uhlovodíků
**'''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
**'''Elektrofilní substituce''' – typická reakce aromatických uhlovodíků, při níž reagují s elektrofilním činidlem, které vzniká během reakce, př. nitrace arenů (nitroskupina NO<sub>2</sub> v podobě nitroniového kationtu se zavádí do molekuly arenu)
**'''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 NO<sub>2</sub> in the form of a nitronium cation is introduced into the arene molecule)
**'''Nukleofilní substituce''' – nukleofilní činidlo reaguje s uhlíkovým atomem a částečně kladným nábojem, reakce je typická pro alkyhalogenidy
**'''Nucleophilic substitution''' – a nucleophilic reagent reacts with a carbon atom and a partially positive charge, the reaction is typical for alkyl halides


===Přesmyk===
===Permutation===


*izomerační reakce, při níž dochází k přeskupení atomů uvnitř molekuly
*Isomerization reaction in which the atoms inside the molecule are rearranged


==Typy reakcí podle počtu fází==
===Homogenní===


*reakce, při nichž jsou reaktanty v jedné fázi, nejčastěji plynné nebo kapalné, např. H<sub>2</sub> (g) + I<sub>2</sub> (g) → 2 HI (g)
==Types of reactions according to the number of phases==
===Homogeneous===


===Heterogenní===
*Reactions in which the reactants are in one phase, most often gaseous or liquid, e.g. H<sub>2</sub> (g) + I<sub>2</sub> (g) → 2 HI (g)


*reakce, při nichž jsou reaktanty v různých fázích a reakce probíhá na jejich fázovém rozhraní, např. 2 HCl (aq) + Zn (s) → ZnCl<sub>2</sub> (aq) + H<sub>2</sub> (g)
===Heterogeneous===


==Typy reakcí podle druhu přenášených částic==
*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) → ZnCl<sub>2</sub> (aq) + H<sub>2</sub> (g)
===Oxidačně – redukční===


*redoxní
==Types of reactions according to the type of transferred particles==
*reakce, při nichž dochází k přenosu elektronů mezi reakčními složkami, probíhající jako dvě dílčí reakce – oxidace a redukce; určité atomy elektrony odevzdávají, tím se oxidují, a současně jiné atomy elektrony přijímají, tím se redukují
===Oxidation-reduction===


===Acidobazické===
*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


*protolytické
===Acid-base===
*reakce, při nichž dochází k přenosu kationtu H<sup>+</sup>; látky odštěpující kation H<sup>+</sup> nazýváme kyseliny, látky přijímající kation H<sup>+</sup> nazýváme zásady (dle Brönsted-Lowryho teorie kyselin a zásad)


===Koordinační===
*protolytic
*reactions in which the cation H<sup>+</sup> is transferred ; substances that donate H<sup>+</sup> cations are called acids, substances that accept H<sup>+</sup> cations are called bases (according to the Brönsted-Lowry theory of acids and bases)


*komplexotvorné
===Coordination===
*reakce, při nichž dochází k přenosu celých skupin atomů a vzniku koordinačních (komplexních) sloučenin


==Typy reakcí podle způsobu štěpení vazeb==
*complex forming
===Homolytické===
*reactions during which whole groups of atoms are transferred and complex compounds are formed


*reakce, při nichž se kovalentní vazba tvořená atomy se stejnou (nebo téměř stejnou) elektronegativitou štěpí symetricky tak, že každá ze vzniklých částic si nechá jeden elektron a vytvoří radikály, např. Cl – Cl → Cl ∙ + Cl ∙
==Types of reactions according to the method of bond cleavage==
===Homolytic===


===Heterolytické===
*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 ∙


*opakem homolýzy
===Heterolytic===
*vazba se štěpí nesymetricky, vázané částice mají velký rozdíl elektronegativit, elektronegativnější částice si ponechá celý elektronový pár z vazby a vznikají ionty, např. HCl → H<sup>+</sup> + Cl<sup>-</sup>


==Odkazy==
*the opposite of homolysis
===Související články===
*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<sup>+</sup> + Cl<sup>-</sup>


* [[Chemická rovnováha]]
==Links==
===Related articles===


===Požitá literatura===
* [[Chemical equilibrium]]


* {{Citace
===Literature===
| typ = kniha
 
* {{Cite
| type = book
| isbn = 978-80-246-1414-4
| isbn = 978-80-246-1414-4
| příjmení1 = Slezina
| surname1 = Slezina
| jméno1 = Miroslav
| name1 = Miroslav
| kolektiv = ano
| collective = yes
| titul = Biochemie pro studující medicíny
| title = Biochemie pro studující medicíny
| vydání = 2
| edition = 2
| místo = Praha
| city = Praha
| vydavatel = Karolinum
| publisher = Karolinum
| rok = 2009
| year = 2009
| rozsah = 0
| range = 0
}}
}}


* {{Citace
* {{Cite
| typ = kniha
| type = book
| isbn = 80-862-8556-1
| isbn = 80-862-8556-1
| příjmení1 = Benešová
| surname1 = Benešová
| jméno1 = Marika
| name1 = Marika
| příjmení2 = Satrapová
| surname2 = Satrapová
| jméno2 = Hana
| name2 = Hana
| titul = Odmaturuj! z chemie
| title = Odmaturuj! z chemie
| vydání = 1
| edition = 1
| místo = Brno
| city = Brno
| vydavatel = Didaktis
| publisher = Didaktis
| rok = 0000
| year = 0000
| rozsah = 0
| range = 0
}}
}}


*
{{Zkontrolovat}}


[[Kategorie:Biochemie]]
[[Category:Biochemistry]]
[[Kategorie:Chemie]]
[[Category:Chemistry]]

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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

  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

  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

Synthesis

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

Analysis

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

Single-Replacement Reactions

  • 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

  • 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

Addition

  • 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

  • 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

  • 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

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


Types of reactions according to the number of phases

Homogeneous

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

Heterogeneous

  • 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

Oxidation-reduction

  • 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

  • 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

  • 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

Homolytic

  • 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

  • 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

Related articles

Literature

  • 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.