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  2. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    N-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic addition, and electrophilic substitution reactions in organic chemistry.

  3. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    At room temperature, bromine trifluoride (BrF 3) is a straw-coloured liquid. It may be formed by directly fluorinating bromine at room temperature and is purified through distillation. It reacts violently with water and explodes on contact with flammable materials, but is a less powerful fluorinating reagent than chlorine trifluoride.

  4. Wohl–Ziegler bromination - Wikipedia

    en.wikipedia.org/wiki/Wohl–Ziegler_bromination

    The Wohl–Ziegler reaction [1] [2] is a chemical reaction that involves the allylic or benzylic bromination of hydrocarbons using an N-bromosuccinimide and a radical initiator. [3] Best yields are achieved with N-bromosuccinimide in carbon tetrachloride solvent. Several reviews have been published. [4] [5]

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The process generates a range of ... Alkenes react with N-bromosuccinimide and ... Tertiary alcohols are eliminated easily at just above room temperature, but primary ...

  6. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols. Butanone (methyl ethyl ketone) organic compound; similar solvent properties to acetone but has a significantly slower evaporation rate Butylated hydroxytoluene

  7. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    At room temperature, bromine trifluoride (BrF 3) is a straw-coloured liquid. It may be formed by directly fluorinating bromine at room temperature and is purified through distillation. It reacts violently with water and explodes on contact with flammable materials, but is a less powerful fluorinating reagent than chlorine trifluoride.

  8. Succinimide - Wikipedia

    en.wikipedia.org/wiki/Succinimide

    C 4 H 5 N O 2: Molar mass: 99.089 g·mol −1 Appearance ... N-Bromosuccinimide; References This page was last edited on 25 October 2024, at 15:33 ...

  9. Room temperature - Wikipedia

    en.wikipedia.org/wiki/Room_temperature

    A digital thermometer reading an ambient temperature of 36.4°C (97°F) in an unventilated room during a heat wave; a high indoor temperature can cause heat exhaustion or heat stroke in a person. The World Health Organization in 1987 found that comfortable indoor temperatures of 18–24 °C (64–75 °F) were not associated with health risks ...