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HomeChemical StructureBoron Tribromide Lewis StructureMedia Portfolio Boron Tribromide Lewis Structure Labeled Sulfur Hexafluoride How Many Electrons Are Fluorine Electron Dot Nitrogen Nitric Oxide Number Valence Rules Expanded Octet

Media Portfolio Boron Tribromide Lewis Structure Labeled Sulfur Hexafluoride How Many Electrons Are Fluorine Electron Dot Nitrogen Nitric Oxide Number Valence Rules Expanded Octet

Chemical Structure / July 6, 2018 / Reina Huffman

Media Portfolio Boron Tribromide Lewis Structure Labeled Sulfur Hexafluoride How Many Electrons Are Fluorine Electron Dot Nitrogen Nitric Oxide Number Valence Rules Expanded Octet Chemical

Before You Go

Glyoxal Structure

Glyoxal Structure

Diazomethane Structure

Diazomethane Structure

Primidone Structure

Primidone Structure

Carbonyl Sulfide Lewis Structure

Carbonyl Sulfide Lewis Structure

Diltiazem Structure

Diltiazem Structure

Phenylacetic Acid Structure

Phenylacetic Acid Structure

Acrolein Structure
Acrolein Structure
Benazepril Structure
Benazepril Structure

Mono acyl derivative of o-phenylenediamine is readily converted into the corresponding benzimidazole by the action of heat alone. These conversions are generally carried out at a temperature somewhat above the melting point of the starting compounds. This is a convenient method for preparing benzimidazoles when monoacyl derivatives are easily obtainable. The procedure may be improved by heating the monoacyl derivative of diamine in an atmosphere of nitrogen to prevent oxidation (Kelly, 1945).

Chlorosulfonic acid is a strong acid that is synthesized on an industrial scale by reacting sulfur trioxide and dry hydrogen chloride gas in an equimolar ratio. It can act as a sulfonating, dehydrating, oxidizing and chlorinating agent. It is reported to be a better electrophilic olefin cyclization agent in comparison to other sulfonic acids. Its infrared spectra in the solid, liquid and gaseous state have been recorded in the region 4000-400cm-1.

Gallery Of Boron Tribromide Lewis Structure

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