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  2. Chloramines - Wikipedia

    en.wikipedia.org/wiki/Chloramines

    N-Chloropiperidine is a rare example of an organic chloramine. [5] Chloramine-T is often referred to as a chloramine, but it is really a salt (CH 3 C 6 H 4 SO 2 NClNa) derived from a chloramine. [6] Organic chloramines feature the NCl functional group attached to an organic substituent.

  3. Monochloramine - Wikipedia

    en.wikipedia.org/wiki/Monochloramine

    Monochloramine, often called chloramine, is the chemical compound with the formula NH 2 Cl. Together with dichloramine (NHCl 2 ) and nitrogen trichloride (NCl 3 ), it is one of the three chloramines of ammonia . [ 3 ]

  4. Chlorine-releasing compounds - Wikipedia

    en.wikipedia.org/wiki/Chlorine-releasing_compounds

    Chloramine, NH 2 Cl. This chemical is commonly handled as a dilute aqueous solution. It is used as an alternative to chlorine and sodium hypochlorite for disinfection of drinking water and swimming pools. Chloramine-T, or tosylchloramide sodium salt, [(H 3 C)(C 6 H 4)(SO 2)(NHCl)] − Na +. This solid compound is available in tablet or powder ...

  5. Chloramine-T - Wikipedia

    en.wikipedia.org/wiki/Chloramine-T

    Chloramine-T is harmful if swallowed. It is corrosive on skin, eyes or mucous membranes. It releases toxic chlorine gas upon reaction with acids. It is water-soluble and thus can be released to the environment dissolved in water. It is a known sensitizer. [9] Chloramine-T has been observed to cause occupational asthma and flu-like symptoms. [7 ...

  6. Possibly toxic chemical may be widespread in drinking water ...

    www.aol.com/possibly-toxic-chemical-may...

    A previously unidentified chemical has been discovered in the tap water of about one-third of U.S. homes, a new study has found, and scientists are actively investigating whether it's toxic.

  7. Quinone - Wikipedia

    en.wikipedia.org/wiki/Quinone

    An example of 1,4-addition reaction is the addition of hydrogen chloride to form chlorohydroquinone: 1,4-addition reaction of quinone with hydrogen chloride to produce chlorohydroquinone. Quinones can undergo Diels–Alder reactions. [10] The quinone acts as the dienophile and reacts with a diene at a carbon-carbon double bond.

  8. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    Functional group interconversion can be used in retrosynthetic analysis to plan organic synthesis. A functional group is a group of atoms in a molecule with distinctive chemical properties, regardless of the other atoms in the molecule. The atoms in a functional group are linked to each other and to the rest of the molecule by covalent bonds.

  9. Primary nutritional groups - Wikipedia

    en.wikipedia.org/wiki/Primary_nutritional_groups

    Primary nutritional groups are groups of organisms, divided in relation to the nutrition mode according to the sources of energy and carbon, needed for living, growth and reproduction. The sources of energy can be light or chemical compounds; the sources of carbon can be of organic or inorganic origin.