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  2. Dyson Perrins Laboratory - Wikipedia

    en.wikipedia.org/wiki/Dyson_Perrins_Laboratory

    The entrance. The Dyson Perrins Laboratory is in the science area of the University of Oxford and was the main centre for research into organic chemistry of the University from its foundation in 1916 until its closure as a research laboratory in 2003. [1]

  3. R. H. A. Plimmer - Wikipedia

    en.wikipedia.org/wiki/R._H._A._Plimmer

    Organic and Bio-Chemistry (originally entitled Practical Physiological Chemistry and later Practical Organic and Bio-chemistry; Longmans, Green and Co., six editions in 1910–38) [19] [32] Analyses and Energy Values of Foods (H. M. Stationery Office; 1921) The History of the Biochemical Society 1911–1949 (Cambridge University Press; 1949)

  4. List of chemical databases - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_databases

    organic chemicals reaction pathway calculation; Beilstein CAS SMILES proprietary 7,000,000 ChEMBL: Chemicals from European Molecular Biology Laboratory EMBL: molecules with drug-like properties "ChEMBL". 1,961,000 cheML.io: Departments of Computer Science and Chemistry at Nazarbayev University de novo molecules generated by ML models

  5. A value - Wikipedia

    en.wikipedia.org/wiki/A_value

    A-values can help predict the steric effect of a substituent. In general, the larger a substituent's A-value, the larger the steric effect of that substituent. A methyl group has an A-value of 1.74 while tert-butyl group has an A-value of ~5. Because the A-value of tert-butyl is higher, tert-butyl has a larger steric effect than methyl. This ...

  6. Good's buffers - Wikipedia

    en.wikipedia.org/wiki/Good's_buffers

    Good's buffers (also Good buffers) are twenty buffering agents for biochemical and biological research selected and described by Norman Good and colleagues during 1966–1980. [ 1 ] [ 2 ] [ 3 ] Most of the buffers were new zwitterionic compounds prepared and tested by Good and coworkers for the first time, though some ( MES , ADA , BES , Bicine ...

  7. Oleum - Wikipedia

    en.wikipedia.org/wiki/Oleum

    The value of y can be varied, to include different oleums. They can also be described by the formula H 2 SO 4 ·xSO 3 where x is now defined as the molar free sulfur trioxide content. Oleum is generally assessed according to the free SO 3 content by mass. It can also be expressed as a percentage of sulfuric acid strength; for oleum ...

  8. Organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_chemistry

    Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1]

  9. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; 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.

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