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Hydrogen complementary

The catalyst, which may be regarded as complementary to Raney nickel (Section VI,5) is largely used for the hydrogenation of esters (esters of monobasic and of dibasic acids to alcohols and glycols respectively) ... [Pg.872]

Figure 6 4 shows the complementary nature of the electrostatic potentials of an alkene and a hydrogen halide We also know (from Section 4 8) that carbocations when gen erated m the presence of halide anions react with them to form alkyl halides... [Pg.236]

Many biological processes involve an associa tion between two species in a step prior to some subsequent transformation This asso ciation can take many forms It can be a weak associ ation of the attractive van der Waals type or a stronger interaction such as a hydrogen bond It can be an electrostatic attraction between a positively charged atom of one molecule and a negatively charged atom of another Covalent bond formation between two species of complementary chemical re activity represents an extreme kind of association It often occurs in biological processes in which aide hydes or ketones react with amines via imine inter mediates... [Pg.728]

Also present in the first test tube is a synthetic analog of ATP in which both the 2 and 3 hydroxyl groups have been replaced by hydrogens This compound is called 2 3 dideoxyadenosme triphosphate (ddATP) Similarly ddTTP is added to the second tube ddGTP to the third and ddCTP to the fourth Each tube also contains a primer The primer is a short section of the complementary DNA strand which has been labeled with a radioactive isotope of phosphorus ( P) When the electrophoresis gel is examined at the end of the experiment the positions of the DNAs formed by chain extension of the primer are located by a technique called autoradiography which detects the particles emitted by the P isotope... [Pg.1181]

Section 28 8 The most common form of DNA is B DNA which exists as a right handed double helix The carbohydrate-phosphate backbone lies on the outside the punne and pyrimidine bases on the inside The double helix IS stabilized by complementary hydrogen bonding (base pairing) between adenine (A) and thymine (T) and guanine (G) and cytosine (C)... [Pg.1188]

Dou ble hel ix (Section 28 8) The form in which DNA normally occurs in living systems Two complementary strands of DNA are associated with each other by hydrogen bonds be tween their base pairs and each DNA strand adopts a helical shape... [Pg.1281]

Fig. 31. Supramolecular (hydrogen-bonded) motifs of self-complementary molecules (196). Fig. 31. Supramolecular (hydrogen-bonded) motifs of self-complementary molecules (196).
Fluorocarbons are made commercially also by the electrolysis of hydrocarbons in anhydrous hydrogen fluoride (Simons process) (14). Nickel anodes and nickel or steel cathodes are used. Special porous anodes improve the yields. This method is limited to starting materials that are appreciably soluble in hydrogen fluoride, and is most useflil for manufacturing perfluoroalkyl carboxyflc and sulfonic acids, and tertiary amines. For volatile materials with tittle solubility in hydrofluoric acid, a complementary method that uses porous carbon anodes and HF 2KF electrolyte (Phillips process) is useflil (14). [Pg.283]

The two most commonly applied systems for naming polycyclic parents are in some ways complementary. Fusion nomenclature provides names for structures containing the maximum number of non-cumulative double bonds von Baeyer nomenclature (Section 1.02.3.4) names fully saturated structures. Thus names for partially hydrogenated structures can be arrived at either by adding hydro prefixes to fusion names or ene , diene , etc. suffixes to von Baeyer names (see examples 29 and 30). If needed, rules are available for... [Pg.20]

In conclusion, one important factor that contributes to the strong affinity of TBP proteins to TATA boxes is the large hydrophobic interaction area between them. Major distortions of the B-DNA structure cause the DNA to present a wide and shallow minor groove surface that is sterically complementary to the underside of the saddle structure of the TBP protein. The complementarity of these surfaces, and in addition the six specific hydrogen bonds between four side chains from TBP and four hydrogen bond acceptors from bases in the minor groove, are the main factors responsible for causing TBP to bind to TATA boxes 100,000-fold more readily than to a random DNA sequence. [Pg.158]


See other pages where Hydrogen complementary is mentioned: [Pg.52]    [Pg.343]    [Pg.1166]    [Pg.1168]    [Pg.1169]    [Pg.1188]    [Pg.63]    [Pg.181]    [Pg.181]    [Pg.182]    [Pg.191]    [Pg.193]    [Pg.207]    [Pg.210]    [Pg.210]    [Pg.241]    [Pg.421]    [Pg.62]    [Pg.73]    [Pg.249]    [Pg.255]    [Pg.260]    [Pg.197]    [Pg.210]    [Pg.4]    [Pg.245]    [Pg.99]    [Pg.95]    [Pg.147]    [Pg.147]    [Pg.157]    [Pg.199]    [Pg.201]    [Pg.500]    [Pg.690]    [Pg.16]    [Pg.334]    [Pg.299]    [Pg.913]    [Pg.668]   
See also in sourсe #XX -- [ Pg.18 , Pg.33 , Pg.38 ]

See also in sourсe #XX -- [ Pg.224 ]




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Complementariness

Complementary

Complementary hydrogen bond

Complementary hydrogen bonding

Complementary hydrogen-bonded double

Complementary hydrogen-bonded double helix

Complementary intermolecular hydrogen

Complementary intermolecular hydrogen bonding

Hydrogen bonding between complementary

Hydrogen bonding between complementary base pairs

Hydrogen bonding self-complementary motifs

Hydrogen self complementary

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