enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Bromate - Wikipedia

    en.wikipedia.org/wiki/Bromate

    3, is a bromine-based oxoanion. A bromate is a chemical compound that contains this ion. Examples of bromates include sodium bromate (NaBrO 3) and potassium bromate (KBrO 3). Bromates are formed many different ways in municipal drinking water. The most common is the reaction of ozone and bromide: Br − + O 3 → BrO − 3

  3. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2. It is a colourless, flammable gas with a faint "sweet and musky " odour when pure. [ 7 ] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds ).

  4. Bromide - Wikipedia

    en.wikipedia.org/wiki/Bromide

    Bromine readily reacts with water, i.e. it undergoes hydrolysis: Br 2 + H 2 O → HOBr + HBr. This forms hypobromous acid (HOBr), and hydrobromic acid (HBr in water). The solution is called "bromine water". The hydrolysis of bromine is more favorable in the presence of base, for example sodium hydroxide: Br 2 + NaOH → NaOBr + NaBr

  5. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The anion reacts with bromine in an α-substitution reaction to give an N-bromoamide. Base abstraction of the remaining amide proton gives a bromoamide anion. The bromoamide anion rearranges as the R group attached to the carbonyl carbon migrates to nitrogen at the same time the bromide ion leaves, giving an isocyanate.

  6. Ionic bonding - Wikipedia

    en.wikipedia.org/wiki/Ionic_bonding

    The oppositely charged ions – typically a great many of them – are then attracted to each other to form solid sodium fluoride. Ionic bonding is a type of chemical bonding that involves the electrostatic attraction between oppositely charged ions , or between two atoms with sharply different electronegativities , [ 1 ] and is the primary ...

  7. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    Many syntheses have been developed. One popular route entails reduction of benzoin using zinc amalgam. [6]C 6 H 5 –CH(OH)–C(=O)–C 6 H 5, trans-C 6 H 5 –CH=CH–C 6 H 5. Both isomers of stilbene can be produced by decarboxylation of α-phenylcinnamic acid, trans-stilbene being produced from the (Z)-isomer of the acid.

  8. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    These compounds usually form the -1, +1, +3 and +5 oxidation states. Bromine is intermediate in reactivity between chlorine and iodine, and is one of the most reactive elements. Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger ...

  9. Electrophile - Wikipedia

    en.wikipedia.org/wiki/Electrophile

    For example, ethene + bromine → 1,2-dibromoethane: C 2 H 4 + Br 2 → BrCH 2 CH 2 Br. This takes the form of 3 main steps shown below; [3] Forming of a π-complex The electrophilic Br-Br molecule interacts with electron-rich alkene molecule to form a π-complex 1. Forming of a three-membered bromonium ion