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A single-displacement reaction, also known as single replacement reaction or exchange reaction, is an archaic concept in chemistry. It describes the stoichiometry of some chemical reactions in which one element or ligand is replaced by atom or group. [1] [2] [3] It can be represented generically as: + +
A neutralization reaction is a type of double replacement reaction. A neutralization reaction occurs when an acid reacts with an equal amount of a base. This reaction usually produces a salt. One example, hydrochloric acid reacts with disodium iron tetracarbonyl to produce the iron dihydride: 2 HCl + Na 2 Fe(CO) 4 → 2 NaCl + H 2 Fe(CO) 4
Chemical decomposition, or chemical breakdown, is the process or effect of simplifying a single chemical entity (normal molecule, reaction intermediate, etc.) into two or more fragments. [1] Chemical decomposition is usually regarded and defined as the exact opposite of chemical synthesis .
A thermite reaction using iron(III) oxide. The sparks flying outwards are globules of molten iron trailing smoke in their wake. A chemical reaction is a process that leads to the chemical transformation of one set of chemical substances to another. [1]
Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...
Atmospheric electricity utilization for the chemical reaction in which water is separated into oxygen and hydrogen. (Image via: Vion, US patent 28793. June 1860.) Electrolyser front with electrical panel in foreground. Electrolysis of water is the decomposition of water (H 2 O) into oxygen (O 2) and hydrogen (H 2): [2] Water electrolysis ship ...
The Bamford–Stevens reaction has not proved useful for the stereoselective generation of alkenes via thermal decomposition of metallated tosylhydrazones due to the indiscriminate 1,2-rearrangement of the carbene center, which gives a mixture of products. By replacing an alkyl group with a trimethylsilyl (TMS) group on N-aziridinylimines ...
In organic chemistry, the E i mechanism (Elimination Internal/Intramolecular), also known as a thermal syn elimination or a pericyclic syn elimination, is a special type of elimination reaction in which two vicinal (adjacent) substituents on an alkane framework leave simultaneously via a cyclic transition state to form an alkene in a syn elimination. [1]