Chloroform and Dichlorocarbene

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Chloroform and Dichlorocarbene

Chloroform vs. Dichlorocarbene

Chloroform, or trichloromethane, is an organic compound with formula CHCl3. Dichlorocarbene is the reactive intermediate with chemical formula CCl2.

Alkene

In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.

Alkene and Chloroform · Alkene and Dichlorocarbene · See more »

Carbon tetrachloride

Carbon tetrachloride, also known by many other names (the most notable being tetrachloromethane, also recognized by the IUPAC, carbon tet in the cleaning industry, Halon-104 in firefighting, and Refrigerant-10 in HVACR) is an organic compound with the chemical formula CCl4.

Carbon tetrachloride and Chloroform · Carbon tetrachloride and Dichlorocarbene · See more »

Chemical formula

A chemical formula is a way of presenting information about the chemical proportions of atoms that constitute a particular chemical compound or molecule, using chemical element symbols, numbers, and sometimes also other symbols, such as parentheses, dashes, brackets, commas and plus (+) and minus (−) signs.

Chemical formula and Chloroform · Chemical formula and Dichlorocarbene · See more »

Cyclopropane

Cyclopropane is a cycloalkane molecule with the molecular formula C3H6, consisting of three carbon atoms linked to each other to form a ring, with each carbon atom bearing two hydrogen atoms resulting in D3h molecular symmetry.

Chloroform and Cyclopropane · Cyclopropane and Dichlorocarbene · See more »

Dichloromethane

Methylene dichloride (DCM, or methylene chloride, or dichloromethane) is a geminal organic compound with the formula CH2Cl2.

Chloroform and Dichloromethane · Dichlorocarbene and Dichloromethane · See more »

Phase-transfer catalyst

In chemistry, a phase-transfer catalyst or PTC is a catalyst that facilitates the migration of a reactant from one phase into another phase where reaction occurs.

Chloroform and Phase-transfer catalyst · Dichlorocarbene and Phase-transfer catalyst · See more »

Reimer–Tiemann reaction

The Reimer–Tiemann reaction is a chemical reaction used for the ortho-formylation of phenols; with the simplest example being the conversion of phenol to salicylaldehyde.

Chloroform and Reimer–Tiemann reaction · Dichlorocarbene and Reimer–Tiemann reaction · See more »

Sodium hydroxide

Sodium hydroxide, also known as lye, is an inorganic compound with the formula NaOH. It is a white solid ionic compound consisting of sodium cations and hydroxide anions. Sodium hydroxide is a highly caustic base and alkali that decomposes proteins at ordinary ambient temperatures and may cause severe chemical burns. It is highly soluble in water, and readily absorbs moisture and carbon dioxide from the air. It forms a series of hydrates NaOH·n. The monohydrate NaOH· crystallizes from water solutions between 12.3 and 61.8 °C. The commercially available "sodium hydroxide" is often this monohydrate, and published data may refer to it instead of the anhydrous compound. As one of the simplest hydroxides, it is frequently utilized alongside neutral water and acidic hydrochloric acid to demonstrate the pH scale to chemistry students. Sodium hydroxide is used in many industries: in the manufacture of pulp and paper, textiles, drinking water, soaps and detergents, and as a drain cleaner. Worldwide production in 2004 was approximately 60 million tonnes, while demand was 51 million tonnes.

Chloroform and Sodium hydroxide · Dichlorocarbene and Sodium hydroxide · See more »

Sodium hypochlorite

No description.

Chloroform and Sodium hypochlorite · Dichlorocarbene and Sodium hypochlorite · See more »