enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. National Council of Educational Research and Training

    en.wikipedia.org/wiki/National_Council_of...

    Those who wish to adopt the textbooks are required to send a request to NCERT, upon which soft copies of the books are received. The material is press-ready and may be printed by paying a 5% royalty, and by acknowledging NCERT. [11] The textbooks are in color-print and are among the least expensive books in Indian book stores. [11]

  3. 6-Diazo-5-oxo-L-norleucine - Wikipedia

    en.wikipedia.org/wiki/6-Diazo-5-oxo-L-norleucine

    Solutions of at least 50 μM DON in 0.9% NaCl are lightly yellowish. The crystalline form appears as yellowish greenish needles. The specific rotation is [α] 26 D +21° (c = 5.4% in H 2 O). In phosphate buffer, pH 7 are the ultraviolet absorption maxima at 274 nm (E1%1 cm. 683) and 244 nm (E1%1 cm 376). [3] [6]

  4. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    Acetic acid, CH 3 COOH, is an acid because it donates a proton to water (H 2 O) and becomes its conjugate base, the acetate ion (CH 3 COO −). H 2 O is a base because it accepts a proton from CH 3 COOH and becomes its conjugate acid, the hydronium ion, (H 3 O +). [9]

  5. SWAYAM - Wikipedia

    en.wikipedia.org/wiki/SWAYAM

    A local chapter will be under one faculty member of the college as one Single Point of Contact (SPOC). Further under the SWAYAM-NPTEL webpage, two more departments are operated, i.e., timeline, list of active local chapters, local chapter ratings, etc. Other departments show news from local chapters, i.e., local chapter colleges/universities.

  6. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    Hydroformylation of an alkene (R 1 to R 3 organyl groups (i. e. alkyl-or aryl group) or hydrogen). In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2).

  7. Gattermann reaction - Wikipedia

    en.wikipedia.org/wiki/Gattermann_reaction

    The Gattermann reaction (also known as the Gattermann formylation and the Gattermann salicylaldehyde synthesis) is a chemical reaction in which aromatic compounds are formylated by a mixture of hydrogen cyanide (HCN) and hydrogen chloride (HCl) in the presence of a Lewis acid catalyst such as aluminium chloride (AlCl 3). [1]

  8. Hunsdiecker reaction - Wikipedia

    en.wikipedia.org/wiki/Hunsdiecker_reaction

    The reaction is named after Cläre Hunsdiecker and her husband Heinz Hunsdiecker, whose work in the 1930s [5] [6] developed it into a general method. [1]The reaction was first demonstrated by Alexander Borodin in 1861 in his reports of the preparation of methyl bromide (CH 3 Br) from silver acetate (CH 3 CO 2 Ag).

  9. Ketene - Wikipedia

    en.wikipedia.org/wiki/Ketene

    The angle between the two H atoms is 121.5°, similar to the theoretically ideal angle formed in alkenes between sp 2 carbon atom and H substituents. [5] Ketenes are unstable and cannot be stored. In the absence of nucleophiles with which to react, ethenone dimerises to give β-lactone, a cyclic ester. If the ketene is disubstituted, the ...