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Normal reactions

To 2 ml. of the ester, add 2--3 drops of a saturated freshly prepared solution of scdium bisulphite. On shaking, a gelatinous precipitate of the bisulphite addition product (D) of the keto form separates, and on standing for 5-10 minutes usually crystallises out. This is a normal reaction of a ketone (see p. 344) hydrogen cyanide adds on similarly to give a cyanhydrin. [Pg.269]

Section 8 13 When nucleophilic substitution is used for synthesis the competition between substitution and elimination must be favorable However the normal reaction of a secondary alkyl halide with a base as strong or stronger than hydroxide is elimination (E2) Substitution by the Sn2 mechanism predominates only when the base is weaker than hydroxide or the alkyl halide is primary Elimination predominates when tertiary alkyl halides react with any anion... [Pg.355]

The chemistry of furfuryl alcohol polymerization has received much attention over the years. Several recent reviews have been written (5,6,54). Based on the accumulated data, furfuryl alcohol has to be considered a bifimctional monomer in the initial stage and its "normal" reactions give linear chains or oligomers containing essentially two repeating units (15,16) with (16) predominating. [Pg.79]

Reactions with Amines and Amides. Hydroxybenzaldehydes undergo the normal reactions with aUphatic and aromatic primary amines to form imines and Schiff bases reaction with hydroxylamine gives an oxime, reaction with hydrazines gives hydrazones, and reactions with semicarbazide give semicarbazones. The reaction of 4-hydroxybenzaldehyde with hydroxylamine hydrochloride is a convenient method for the preparation of 4-cyanophenol (52,53). [Pg.505]

Dextrose yield, however, can be increased by conducting saccharification at a lower soHds level where the reverse reaction is minimized. Eor instance, dextrose yields of 98.8, 98.2, 97.5, and 96.9% dry basis can be achieved at soHds levels of 10, 15, 20, and 25%, respectively (10). Low soHds operation, however, is not used commercially owing to problems associated with microbial contamination and cost of water removal. Dextrose level can be increased by 0.5—1.5% at normal reaction soHds by using an enzyme such as puUulanase (11) or a B. megaterium amylase (12) in conjunction with... [Pg.290]

Carboxylic acid derivatives on pyridopyrimidine rings appear to undergo normal reactions with electrophilic reagents, e.g. the 6-amide (70) is dehydrated to the 6-nitrile with phosphorus oxychloride. [Pg.210]

In most other reactions the azolecarboxylic acids and their derivatives behave as expected (cf. Scheme 52) (37CB2309), although some acid chlorides can be obtained only as hydrochlorides. Thus imidazolecarboxylic acids show the normal reactions they can be converted into hydrazides, acid halides, amides and esters, and reduced by lithium aluminum hydride to alcohols (70AHC(12)103). Again, thiazole- and isothiazole-carboxylic acid derivatives show the normal range of reactions. [Pg.92]

Diazotization of aminoazoles with free cyclic NH groups can give diazo anhydrides which show many of the normal reactions of diazoniums (67AHC(8U). In the pyrazole series these diazo anhydrides are particularly stable. [Pg.96]

Metalloid azoles frequently show expected properties, especially if not too many heteroatoms are present. Thus Grignard reagents prepared from halogen-azoles (see Section 4.02.3.9.3) show normal reactions, as in Scheme 60. 2-Lithioimidazoles react normally, e.g. with acetaldehyde (Scheme 61) (70AHC(12)103) 5-lithioisothiazoles (see Scheme 62) (72AHC(14)1) and 2-lithiothiazoles undergo many of the expected reactions. [Pg.106]

The contradictory observations that 16-dehydropregnenolone oxime fails to rearrange with phosphorus oxychloride while pregnenolone oxime undergoes the normal reaction " remain unexplained. The respective 3-acetates in both series rearrange in the expected fashion. [Pg.142]

By agreement between the workers who have introduced these terms, a-values are now generally called a, a, and for the values applicable to normal reactions and to reactions calling strongly for — M and -f M effects, respectively. [Pg.211]

Normal reactions are found again for systems containing C=N double bonds. An unstable triazoline is probably an intermediate product in the reaction of pteridin-7-one (117)to give a mixture of the 8-methyl (118) and 6,8-dimethyl derivatives (119). C-Methylation also occurs in the case of quinoxalin-2-one. ... [Pg.285]

Anxiety is a normal reaction. Pathological anxiety interferes with daily-life activities and may be accompanied by autonomic symptoms (chest pain, dyspnoea and palpitations). Severe forms include phobic anxiety and panic disorder. [Pg.201]

The oxidative addition of silanes (with silicon-hydrogen bonds) to coordinatively unsaturated metal complexes is one of the most elegant methods for the formation of metal-silicon bonds. Under this heading normally reactions are considered which yield stable silyl metal hydrides. However, in some cases the oxidative addition is accompanied by a subsequent reductive elimination of, e.g., hydrogen, and only the products of the elimination step can be isolated. Such reactions are considered in this section as well. [Pg.14]

A so-called abnormal Claisen rearrangement has been observed on a number of occasions usually concurrently with the normal reaction. Here the /1-carbon atom in the ether becomes bonded to the ortho position in the phenyl group as in the formation of C from XCIX139, viz. ... [Pg.473]

A plot illustrating that the order with respect to [H+] varies with [H+] during the reaction in which water is substituted for chloride ion in the complex (H20)5CrCl2+, Eq. (1-16). The ordinate shown is the (normalized) reaction rate, as in Eq. (1-18), and the abscissa is [H+], Both quantities are displayed on logarithmic scales. The apparent reaction orders with respect to [H+] are the limiting slopes, -1 at low [H+] and 0 at high [H+],... [Pg.7]

Incorrect vessel charge either due to automatic control failure or plant operator error could result in excess catalyst or reactant concentration, etc. This could cause a rapidly accelerating reaction rate or could initiate unexpected side reactions, which could be more severe than the normal reaction. [Pg.328]

B. Defining the Reaction Kinetics and Component Physical Properties. The rate expression needed for use in a vent design model should represent the condition that would exist during the emergency. Kinetic data based on the normal reaction rate are only useful in cases when loss of heat transfer can be experienced. [Pg.332]

Glycogenosis type VIII (phosphorylase b kinase deficiency) gives rise to myopathy and liver disease, either singly or in combination. Phosphorylase b kinase (PBK) converts the inactive b form of both muscle and liver phosphorylases to the active a forms of the enzymes. The ischemic lactate test sometimes shows a flat result as in McArdle s disease, but is more likely to be normal. Histochemical demonstration of myophosphorylase activity in tissue sections shows a near-normal reaction due to the presence of phosphorylase a. Accumulation of glycogen is modest and found mainly in type 2 (fast-twitch glycolytic) muscle fibers. [Pg.302]

In comparison to the normal reaction without additive which affords a yield of 50.2 % in phenol, the additives on the right part of the table reduce the induction time probably by trapping more or less efficiently the air-oxygen inhibitor. [Pg.256]

While the action of various accelerators is not altogether clear, many of them (tetramethylthiuram disulfide, for example) may decompose with the release of radicals which accelerate step (i). Others (e.g., the diphenylguanidine type) appear to promote the normal reactions of sulfur, perhaps by catalyzing the conversion of cyclic sulfur (Ss) to a more soluble and reactive form.2 >27 efficiency of sulfur utiliza-... [Pg.456]

As the final proton transfer cannot occur when a-substituted esters are used, such compounds do not condense under the normal reaction conditions, but this limitation... [Pg.149]

By now, I hope that I have convinced you that much of what has passed for common wisdom about depression and antidepressants is simply wrong. Depression is not caused by a chemical imbalance in the brain, and it is not cured by medication. Depression may not even be an illness at all. Often, it can be a normal reaction to abnormal situations. Poverty, unemployment, and the loss of loved ones can make people depressed, and these social and situational causes of depression cannot be changed by drugs. [Pg.177]

Normal Reaction of Water with CUSO4 in Non-hydrolysed State... [Pg.233]

From the above, it could be observed that ultrasound broke down the agglomerated precipitate of Ni-DMG complex to very fine particles, resulting in the formation of colloidal solution of Ni-DMG complex in the presence of an ultrasonic held. The settlement of particles was slow in the sonicated sample than in control sample. However, in the normal reaction, green precipitate of nickel (II) hydroxide dissolved in the excess NH3 solution and formed deep blue solution of hexammi-nenickel(II) ions, as under ... [Pg.241]

In another experiment, different volumes (2.5, 5.0 and 10.0 ml) of 4,000 ppm solution of sodium acetate was added to 10.0 ml of 1,000 ppm solution of aluminium sulphate. In the normal reaction, no precipitate was obtained in cold and neutral solutions, but on boiling with excess reagent, a voluminous precipitate of basic aluminium acetate, Al(OH)2COOCH3, was formed. [Pg.255]


See other pages where Normal reactions is mentioned: [Pg.126]    [Pg.249]    [Pg.217]    [Pg.165]    [Pg.156]    [Pg.265]    [Pg.130]    [Pg.227]    [Pg.832]    [Pg.990]    [Pg.999]    [Pg.712]    [Pg.53]    [Pg.232]    [Pg.320]    [Pg.717]    [Pg.1050]    [Pg.2091]    [Pg.79]    [Pg.203]    [Pg.286]    [Pg.940]    [Pg.343]   


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Acid-base reactions normality

Addition reaction normal

Butene reactions, normal

Characterizing the Normal Reaction

Diels normal reaction

Diels-Alder reaction normal electron demand

Diels-Alder reactions normal

Diels-Alder reactions with normal electron demand

Metals interfering with normal reaction

Normal Diels-Alder Reactions. Synthesis of Pyrones and Thiopyrans

Normal Micelles Effects on Reaction Rates

Normal hydrogen electrode half-reactions

Normal mode coordinates reaction path

Normal reaction, characterizing

Normal-electron demand reactions

Normalized reaction rate

Oxidation-reduction reactions normality

Pyridine, hydroxyReimer-Tiemann reaction normal

Pyrimidine, hydroxyReimer-Tiemann reaction normal

Quinolines, hydroxyReimer-Tiemann reaction normal

Reimer-Tiemann reaction normal

Safe Normal Operation of Reactions Under Reflux

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