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  2. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals. [6]

  3. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl chloride is prepared industrially by the gas-phase photochemical reaction of toluene with chlorine: [3] C 6 H 5 CH 3 + Cl 2 → C 6 H 5 CH 2 Cl + HCl. In this way, approximately 100,000 tonnes are produced annually. The reaction proceeds by the free radical process, involving the intermediacy of free chlorine atoms. [4]

  4. Solvay process - Wikipedia

    en.wikipedia.org/wiki/Solvay_process

    One idea is to react carbon dioxide, produced perhaps by the combustion of coal, to form solid carbonates (such as sodium bicarbonate) that could be permanently stored, thus avoiding carbon dioxide emission into the atmosphere. [20] [21] The Solvay process could be modified to give the overall reaction: 2 NaCl + CaCO 3 + CO 2 + H 2 O → 2NaHCO ...

  5. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    Grignard compounds are popular reagents in organic synthesis for creating new carboncarbon bonds. For example, when reacted with another halogenated compound R'−X' in the presence of a suitable catalyst , they typically yield R−R' and the magnesium halide MgXX' as a byproduct; and the latter is insoluble in the solvents normally used.

  6. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    When chlorine gas (Cl 2) is irradiated, some of the molecules are split into two chlorine radicals (Cl•), whose free electrons are strongly nucleophilic. One of them breaks a C–H covalent bond in CH 4 and grabs the hydrogen atom to form the electrically neutral HCl.

  7. Standard enthalpy of formation - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_formation

    Carbon disulfide: Gas CS 2: 116.7 Carbon monoxide: Gas CO −110.525 Carbonyl chloride Gas COCl 2: −218.8 Carbon dioxide (un–ionized) Aqueous CO 2 (aq) −419.26 Bicarbonate ion Aqueous HCO 3 – −689.93 Carbonate ion Aqueous CO 3 2– −675.23 Monatomic chlorine Gas Cl 121.7 Chloride ion Aqueous Cl −: −167.2 Chlorine: Gas Cl 2: 0 ...

  8. Cation–π interaction - Wikipedia

    en.wikipedia.org/wiki/Cation–π_interaction

    Cation–π interaction between benzene and a sodium cation.. Cation–π interaction is a noncovalent molecular interaction between the face of an electron-rich π system (e.g. benzene, ethylene, acetylene) and an adjacent cation (e.g. Li +, Na +).

  9. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    A halogen addition reaction is a simple organic reaction where a halogen molecule is added to the carboncarbon double bond of an alkene functional group. [1] The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 ...