Share to: share facebook share twitter share wa share telegram print page

Side reaction

A side reaction is a chemical reaction that occurs at the same time as the actual main reaction, but to a lesser extent. It leads to the formation of by-product, so that the yield of main product is reduced:[1]

P1 is the main product if k1> k2. The by-product P2 is generally undesirable and must be separated from the actual main product (usually in a costly process).

In organic synthesis

B and C from the above equations usually represent different compounds. However, they could also just be different positions in the same molecule.

A side reaction is also referred to as competing reaction[2][3] when different compounds (B, C) compete for another reactant (A). If the side reaction occurs about as often as the main reaction, it is spoken of parallel reactions[4] (especially in the kinetics, see below).

Also there may be more complicated relationships: Compound A could reversibly but quickly react to substance B (with speed k1) or irreversible but slow (k1> k−1 >> k2) to substance C:

Thermodynamic and kinetic product.

Assuming that the reaction to substance C is irreversible, as it is thermodynamically very stable. In this case, B is the kinetic and C is the thermodynamic product of the reaction (see also here).[5][6][7] If the reaction is carried out at low temperatures and stopped after a short time, it is spoken of kinetic control, primarily the kinetic product B would be formed. When the reaction is carried out at high temperatures and for long time (in which case the necessary activation energy for the reaction to C is available, which is progressively formed over time), it is spoken of thermodynamic control; the thermodynamic product C is primarily formed.

Conditions for side reactions

In organic synthesis, elevated temperatures usually lead to more side products. Side products are usually undesirable, therefore low temperatures are preferred ("mild conditions"). The ratio between competing reactions may be influenced by a change in temperature because their activation energies are different in most cases. Reactions with high activation energy can be more strongly accelerated by an increase in temperature than those with low activation energy. Also, the state of equilibrium depends on temperature.[8]

Detection reactions can be distorted by side reactions.

Kinetics

Side reactions are also described in the reaction kinetics, a branch of physical chemistry. Side reactions are understood as complex reaction, since the overall reaction (main reaction + side reaction) is composed of several (at least two) elementary reactions.[9] Other complex reactions are competing reactions, parallel reactions, consecutive reactions, chain reactions, reversible reactions, etc.[10]: 280–291 

If one reaction occurs much faster than the other one (k1 > k2), it (k1) will be called the main reaction, the other one (k2) side reaction. If both reactions roughly of same speed (k1 ≅ k2) is spoken of parallel reactions.[4]

If the reactions and are irreversibly (without reverse reaction), then the ratio of P1 and P2 corresponds to the relative reactivity of B and C compared with A:

See also

References

  1. ^ "side reaction auf merriam-webster.com". Retrieved 2015-08-30.
  2. ^ "Konkurrenzreaktion auf chemgapedia.de". Retrieved 2015-08-30.
  3. ^ "Konkurrenzreaktion auf universal_lexikon.deacademic.com". Retrieved 2015-08-30.
  4. ^ a b "4. Kinetik und Katalyse" (PDF). Retrieved 2015-08-30.
  5. ^ "Kinetische und thermodynamische Kontrolle von chemischen Reaktionen auf Chemgapedia.de". Retrieved 2015-12-06.
  6. ^ John Gilbert; Stephen Martin, Experimental Organic Chemistry: A Miniscale and Microscale Approach (in German)
  7. ^ Robert G. Mortimer (2008), Physical Chemistry (in German), Academic Press
  8. ^ Klaus Schwetlick (2009). Organikum: organisch-chemisches Grundpraktikum (in German) (23rd ed.). Weinheim: Wiley-VCH. p. 156. ISBN 978-3-527-32292-3.
  9. ^ "Komplexe Reaktionen auf spektrum.de". Retrieved 2015-08-30.
  10. ^ Winter, von Claus Czeslik, Heiko Seemann, Roland (2010). Basiswissen Physikalische Chemie (4., aktualisierte Aufl. ed.). Wiesbaden: Vieweg+Teubner Verlag / GWV Fachverlage, Wiesbaden. ISBN 9783834893598.{{cite book}}: CS1 maint: multiple names: authors list (link)
Index: pl ar de en es fr it arz nl ja pt ceb sv uk vi war zh ru af ast az bg zh-min-nan bn be ca cs cy da et el eo eu fa gl ko hi hr id he ka la lv lt hu mk ms min no nn ce uz kk ro simple sk sl sr sh fi ta tt th tg azb tr ur zh-yue hy my ace als am an hyw ban bjn map-bms ba be-tarask bcl bpy bar bs br cv nv eml hif fo fy ga gd gu hak ha hsb io ig ilo ia ie os is jv kn ht ku ckb ky mrj lb lij li lmo mai mg ml zh-classical mr xmf mzn cdo mn nap new ne frr oc mhr or as pa pnb ps pms nds crh qu sa sah sco sq scn si sd szl su sw tl shn te bug vec vo wa wuu yi yo diq bat-smg zu lad kbd ang smn ab roa-rup frp arc gn av ay bh bi bo bxr cbk-zam co za dag ary se pdc dv dsb myv ext fur gv gag inh ki glk gan guw xal haw rw kbp pam csb kw km kv koi kg gom ks gcr lo lbe ltg lez nia ln jbo lg mt mi tw mwl mdf mnw nqo fj nah na nds-nl nrm nov om pi pag pap pfl pcd krc kaa ksh rm rue sm sat sc trv stq nso sn cu so srn kab roa-tara tet tpi to chr tum tk tyv udm ug vep fiu-vro vls wo xh zea ty ak bm ch ny ee ff got iu ik kl mad cr pih ami pwn pnt dz rmy rn sg st tn ss ti din chy ts kcg ve 
Prefix: a b c d e f g h i j k l m n o p q r s t u v w x y z 0 1 2 3 4 5 6 7 8 9 
Kembali kehalaman sebelumnya