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React with

As with distillation, no attempt should be made to carry out any optimization of liquid flow rate, temperature, or pressure at this stage in the design. The separation in absorption is sometimes enhanced by adding a component to the liquid which reacts with the solute. [Pg.84]

Amidines are best made in two stages a nitrile reacts with dry HCl and anhydrous alcohols to give an imidic ester (imino-ether) which yields an amidine with NH3. [Pg.27]

For ionized solvents which do not contain protons a base is a substance which reacts with the acid of that system to give a salt and the solvent. Thus the base KBrp4 reacts with the acid BrFiSbFfi to give the salt KSbF and Brp3 in bromine trifluoride. [Pg.52]

CO. Alkynes will react with carbon monoxide in the presence of a metal carbonyl (e.g. Ni(CO)4) and water to give prop>enoic acids (R-CH = CH-C02H), with alcohols (R OH) to give propenoic esters, RCH CHC02R and with amines (R NH2) to give propenoic amides RCHrCHCONHR. Using alternative catalysts, e.g. Fe(CO)5, alkynes and carbon monoxide will produce cyclopentadienones or hydroquinols. A commercially important variation of this reaction is hydroformyiation (the 0x0 reaction ). [Pg.82]

HCl reacts with rubber to form hydrochlor-inated rubber - also used in paints. [Pg.92]

COT is prepared by the polymerization of ethyne at moderate temperature and pressure in the presence of nickel salts. The molecule is non-planar and behaves as a typical cyclic olefin, having no aromatic properties. It may be catalytically hydrogenated to cyclo-octene, but with Zn and dil. sulphuric acid gives 1,3,6-cyclooclairiene. It reacts with maleic anhydride to give an adduct, m.p. 166 C, derived from the isomeric structure bicyclo-4,2,0-octa-2,4,7-triene(I) ... [Pg.122]

CH2C1 CH2C1. Colourless liquid with an odour like that of chloroform b.p. 84 C. It is an excellent solvent for fats and waxes. Was first known as oil of Dutch chemists . Manufactured by the vapour- or liquid-phase reaction of ethene and chlorine in the presence of a catalyst. It reacts with anhydrous ethano-ales to give ethylene glycol diethanoate and with ammonia to give elhylenediamine, these reactions being employed for the manufacture of these chemicals. It burns only with difficulty and is not decomposed by boiling water. [Pg.134]

C, b.p. 170 C (decomp.), has a characteristic odour. It is the Diels-Alder product of cyclopentadiene reacting with itself, the exo-form being formed most rapidly but the endo-form is thermodynamically favoured. At temperatures above ISO C a retro-Diels-Alder reaction occurs and cyclopentadiene monomer is regenerated see diene reactions. [Pg.135]

CH2=CHC = CCH = CH2. a colourless liquid which turns yellow on exposure to the air it has a distinct garlic-like odour b.p. 83-5°C. Manufactured by the controlled, low-temperature polymerization of acetylene in the presence of an aqueous solution of copper(I) and ammonium chlorides. It is very dangerous to handle, as it absorbs oxygen from the air to give an explosive peroxide. When heated in an inert atmosphere, it polymerizes to form first a drying oil and finally a hard, brittle insoluble resin. Reacts with chlorine to give a mixture of chlorinated products used as drying oils and plastics. [Pg.145]


See other pages where React with is mentioned: [Pg.49]    [Pg.281]    [Pg.11]    [Pg.18]    [Pg.19]    [Pg.19]    [Pg.21]    [Pg.21]    [Pg.23]    [Pg.25]    [Pg.25]    [Pg.27]    [Pg.27]    [Pg.28]    [Pg.30]    [Pg.32]    [Pg.42]    [Pg.52]    [Pg.65]    [Pg.65]    [Pg.65]    [Pg.74]    [Pg.80]    [Pg.81]    [Pg.94]    [Pg.94]    [Pg.94]    [Pg.98]    [Pg.106]    [Pg.106]    [Pg.111]    [Pg.116]    [Pg.133]    [Pg.135]    [Pg.137]    [Pg.139]    [Pg.140]    [Pg.141]    [Pg.141]    [Pg.145]    [Pg.158]    [Pg.160]   
See also in sourсe #XX -- [ Pg.2 , Pg.439 ]




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2.4.6- Triphenylpyridine reacts with

A Cations Ability to React with Water

Acetoacetates reacting with alkyl halides

Acids metals reacting with

Acids reacting with

Acrylates reacting with

Acylium cation reacting with aromatics

Aldehydes can react with alcohols to

Aldehydes can react with alcohols to form hemiacetals

Aldehydes reacting with

Alkanes reacting with halogens

Alkenes react with bromine

Alkyl halides reacting with

Allylic sources reacting with

Aluminum hydrides, 155. reacting with

Amines react with carbonyl compounds

An Anions Ability to React with Water

Analysis of the Reaction Products after Reacting Magnesium with Air

Antibodies reacting with denatured DNA

Antibodies reacting with native DNA

Antigenic Determinants Reacting with Antibody

Aromatics reacting with

Atomic hydrogen reacting with

Atomic hydrogen reacting with carbon

Bases. reacting with

Basic anhydride A metal oxide that reacts with

Borane reacting with

Borohydrides reacting with

C-L Sinks Reacting with Common Sources

Calcium react with proteins

Carbocations reacting with

Carbodiimides reacting with carboxylic acids

Carbonyl groups thiols reacting with

Carboxyl derivatives reacting with

Carboxylic acids reacting with

Channel Flow with Soluble or Rapidly Reacting Walls

Channel flow with rapidly reacting walls

Chemicals that React with Stratospheric Ozone

Chlorine sodium atoms reacting with

Conjugate acceptors reacting with

Copper react with proteins

Cyanide anion reacting with

Diazomethane reacting with

Enones, 367. reacting with

Enzymes reacting with both enantiomeric forms of a substrate

Ester enolates reacting with esters

Ethanol reacting with oxygen

Ethyl alcohol elements reacting with

Flux A substance added to react with

From isocyanate reacted with

Frontier orbitals reacting with electrophiles

Frontier orbitals reacting with radicals

Gasoline oxygen reacting with

Grignard reagents react with boronic acid

H-A Sinks Reacting with Common Sources

How Do Carboxylic Acid Derivatives React with Alcohols

How Do Carboxylic Acid Derivatives React with Ammonia and Amines

How Do Esters React with Grignard Reagents

Hydrocarbons, react with oxygen

Hydrochloric acid zinc reacting with

Hydrogen halides reacting with

Hydrogen peroxide reacting with

Hydrogen reacting with deuterium molecule

Hydroxide ions from base reacting with

Hydroxide reacting with

Hydroxylamines reacting with ketones

Iminium ions reacting with enols

Iron atoms reacting with

Iron atoms reacting with chemistry

Isothiazole react with hexacarbonyls

Ketones alkyne anion reacting with

Ketones organolithium reagent reacting with

Lewis acids reacting with lone pairs

Lone pairs reacting with

Magnesium react with proteins

Major Paths for Radicals Reacting with Neutrals

Materials reacting aggressively with water

Materials which react with cement hydration products

Mercury react with proteins

Metal Complexes which React Irreversibly with Dioxygen

Metal Complexes which React Reversibly with Dioxygen

Metal hydrides reacting with

Metals reacting with gases studied

Methane reacting with water

Ninhydrin react with amino

Ninhydrin react with amino acids

Nitric Oxide Reacting with Superoxide

Nonacarbonyl, diiron, react with

Object reacting with adhesive

Organoboranes reacting with

Organocoppers, 154. reacting with enones

Organolithiums, 154. reacting with enones

Organomagnesiums, 154. reacting with

Organometallics reacting with

Oxygen complexes reacting with

Oxygen metal reacting with

Oxygen methane reacting with

Oxygen propane reacting with

Permanganate, iron ions reacting with

Peroxides reacting with enones

Phosphate esters reacting with hydroxide

Plasma-produced reacting with

Polarized multiple bonds reacting with

Potassium react with proteins

Potassium reacting with water

Potential Electrolytes Nonionic Substances That React with the Solvent to Yield Ions

REACT

React reacted with, reaction

Reacting Metallic Calcium with Carbon

Reacting with Knoevenagel Condensation

Reacting with other elements

Scandium atoms reacting with

Sodium react with proteins

Sulfonyl halides reacting with alcohols

Sulfur ylides reacting with ketones

Synthetic Molecules That Specifically React with Target Sequences

The initial solid reacts with another phase

Thermal analysis metals reacting with gases

Thermodynamic properties complexes reacting with

Thiols arsenical, react with

Vinyl halides from alkynes reacting with acids

Water hazards chemicals reacting with, strong

Water reacting with

Water reacting with strong chemicals

Water, metal reacting with

Y-L Sinks Reacting with Common Sources

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