According to Wikipedia, it's some pretty nasty stuff. They say its "flammable, toxic, and carcinogenic." So basically it blows up, kills you, AND gives you cancer. You may want to check out: http://en.wikipedia.org/wiki/Epichlorohydrin
The infrared (IR) structural frequencies of epichlorohydrin include a strong absorption band around 2930-2980 cm^-1 for aliphatic C-H stretching, a medium absorption band around 1330-1380 cm^-1 for C-O stretching in the epoxide ring, and a strong absorption band around 1030-1090 cm^-1 for C-Cl stretching. These frequencies can vary slightly depending on the specific molecular environment of the molecule.
There are two basic ways glycerol forms. The first is natural, by the combinaation of fats and oils. The second is by sythesizing it, by a cehmical process that begins by chlorinating propylene, which gives allyl chloride, which is oxidized with hypochlorite to dichlorohydrins, which reacts with a strong base to give epichlorohydrin. Epichlorohydrin is then hydrolyzed to give glycerol.
Firstly at 50⁰C in a conventional reactor, mix the reactants (epichlorohydrin and bisphenol A) under a molar ratio of bisphenol A to epicholorhydrin 1:14, then raise the temperature to 115⁰C over a period of time of 30 minutes. Conduct this reaction under a nitrogen gas environment. Secondly add an alkaline catalyst (2 moles of NaOH), as 30% aqueous solution, drop wise. This usually takes several hours. The rate of addition is maintained as such the reaction mixture does not change the colour when phenothalein (an indicator) is added. Thirdly carry out the reaction for an additional 30 minutes and then wash out the excess catalyst. Next raise the temperature to 130⁰C and remove water by decanting (The remaining liquid is dried with anhydrous sodium sulfate or other dessicant) Lastly remove excess epichlorohydrin by vacuum distillation.
You hit it with steam, and it will hydrolyze into phenol and hydrochloric acid. This isn't a real common way of making HCl, though; the chloralkali process that gives us sodium hydroxide also throws off hydrogen and chlorine, which can be mixed and exposed to UV light to give HCl. But as an educational setup, it's fine. Most people get their phenol the old-fashioned way, by oxidizing isopropylbenzene. A big reason for doing it that way is the byproduct of the reaction is acetone. If you condense acetone and phenol, you get bisphenol a, which is required if you want to make either polycarbonate (by reacting it with phosgene) or epoxy (by reacting it with epichlorohydrin). 'Course, you can also sell the acetone and phenol separately because there is great demand for both chemicals.
Since chemistry engages in the composition, properties, and reactions in matter, especially elements, it can help agriculture in that through chemistry we can create new substances to improve our crops, their quality, productivity, and resistance to pests and time. Also through chemistry, accurate proportions of the chemicals used are determined, and the right substances for the crop are known. Hence, chemistry improves agriculture.
The density of epichlorohydrin is approximately 8.6 pounds per gallon. This value can vary slightly depending on temperature and purity, but it generally remains in this range. Always refer to the material safety data sheet (MSDS) or manufacturer specifications for the most accurate information.
The infrared (IR) structural frequencies of epichlorohydrin include a strong absorption band around 2930-2980 cm^-1 for aliphatic C-H stretching, a medium absorption band around 1330-1380 cm^-1 for C-O stretching in the epoxide ring, and a strong absorption band around 1030-1090 cm^-1 for C-Cl stretching. These frequencies can vary slightly depending on the specific molecular environment of the molecule.
L. P. Mendis has written: 'Multicomponent polydiene-epichlorohydrin elastomeric systems'
A simulation in SimSci Pro/II simulator using the NTRL Liquid Activity method at 14.696 psia for 1-chloro-2,3-epoxypropane (epichlorohydrin) and water indicates that they do not. The T-x-y diagram and equilibrium x-y diagrams do not show an azetrope forming at any point. As a side note these two chemicals should be insoluble in one another so you would not generally expect an azeotrope to form. See the link for an image of the equilibrium graphs.
There are two basic ways glycerol forms. The first is natural, by the combinaation of fats and oils. The second is by sythesizing it, by a cehmical process that begins by chlorinating propylene, which gives allyl chloride, which is oxidized with hypochlorite to dichlorohydrins, which reacts with a strong base to give epichlorohydrin. Epichlorohydrin is then hydrolyzed to give glycerol.
Manufacture of Epichlorohydrin which is then used to make epoxy resins.Manufacture of TiCl4 which is then used to make TiO2 a key pigment in paint manufacture and with other uses. TiCl4 is also reacted with sodium metal to produce titanium sponge which is used in aerospace.Manufacture of Phosgene which is used to manufacture isocyanates and polyurethanes.
Firstly at 50⁰C in a conventional reactor, mix the reactants (epichlorohydrin and bisphenol A) under a molar ratio of bisphenol A to epicholorhydrin 1:14, then raise the temperature to 115⁰C over a period of time of 30 minutes. Conduct this reaction under a nitrogen gas environment. Secondly add an alkaline catalyst (2 moles of NaOH), as 30% aqueous solution, drop wise. This usually takes several hours. The rate of addition is maintained as such the reaction mixture does not change the colour when phenothalein (an indicator) is added. Thirdly carry out the reaction for an additional 30 minutes and then wash out the excess catalyst. Next raise the temperature to 130⁰C and remove water by decanting (The remaining liquid is dried with anhydrous sodium sulfate or other dessicant) Lastly remove excess epichlorohydrin by vacuum distillation.
HI! (chlorine is a gas) Principal applications of chlorine are in the production of a wide range of industrial and consumer products. For example, it is used in making plastics, solvents for dry cleaning and metal degreasing, textiles, agrochemicals and pharmaceuticals, insecticides, dyestuffs, household cleaning products, etc. Quantitavely, about 63% and 18% of all chlorine are used in the manufacture of organic and inorganic chlorine compounds, respectively, and about 15,000 chlorine compounds are being used commercially. The remaining 19% is used for bleaches and dissifection products. The most significant of organic compounds in terms of production volume are 1,2-dichloroethane and vinyl chloride, intermediates in the production of PVC. Other particularly important organochlorines are methyl chloride, methylene chloride, chloroform, vinylidene chloride, trichloroethylene, perchloroethylene, allyl chloride, epichlorohydrin, chlorobenzene, dichlorobenzenes, and trichlorobenzenes. The major inorganic compounds include HCl, Cl2O, HOCl, NaClO3, chlorinated isocyanurates, AlCl3, SiCl4, SnCl4, PCl3, PCl5, POCl3, AsCl3, SbCl3, SbCl5, BiCl3, S2Cl2, SCl2, SOCI2, CIF3, ICl, ICl3, TiCl3, TiCl4, MoCl5, FeCl3, ZnCl2, etc. IT IS WIDELY USED IN PURIFING WATER. if you like my answer please send me message at lovely zoya zoya facebook.com GOOD LUCK!
You hit it with steam, and it will hydrolyze into phenol and hydrochloric acid. This isn't a real common way of making HCl, though; the chloralkali process that gives us sodium hydroxide also throws off hydrogen and chlorine, which can be mixed and exposed to UV light to give HCl. But as an educational setup, it's fine. Most people get their phenol the old-fashioned way, by oxidizing isopropylbenzene. A big reason for doing it that way is the byproduct of the reaction is acetone. If you condense acetone and phenol, you get bisphenol a, which is required if you want to make either polycarbonate (by reacting it with phosgene) or epoxy (by reacting it with epichlorohydrin). 'Course, you can also sell the acetone and phenol separately because there is great demand for both chemicals.
Since chemistry engages in the composition, properties, and reactions in matter, especially elements, it can help agriculture in that through chemistry we can create new substances to improve our crops, their quality, productivity, and resistance to pests and time. Also through chemistry, accurate proportions of the chemicals used are determined, and the right substances for the crop are known. Hence, chemistry improves agriculture.
A list of all nouns that start with "e" is not possible in this format. A list of examples of nouns that start with "e" are: eagle eagle-buzzard eagle-owl eagle hawk eagerness ear ear buds ear drum ear lobe ear piece ear plugs ear ring ear tag earl earlobe earmuffs earphones earpiece earring ear earth earth apple earth hog earth pig earthenware earthling earthworm earwax earwig easel Easter bunny Easter egg Easter flower eastern phoebe eatery ebony echidna echinacea echinoderm echo-cardiogram echo-cardiograph eclair ecologist economist ecstasy ectoplasm edge edger editor education educator eel effect effervescence effigy effort egg egg beater egg carton egg cooker egg cup egg custard egg poacher egg roll egg timer egg white eggnog eggplant eggs egress egret Egyptolog Egyptologist eider eiderdown eight ball eight iron eighteen wheeler Einstein eland elastic elbow elbow pads elbow macaroni elder tree elderberry elderberry electric blanket electric chair electric current electric eel electric guitar electric mixer electric organ electric razor electric toothbrush electrical engineer electrical outlet electrical socket electrical storm electrical tape electrician election electricity electrodes electrologist electrolyte electromagnet electron elephant elephant seal elevator elevator mechanic elf elixir Elizabeth II elk elk calf elliptical elliptical machine elliptical trainer elm elm tree elution elver elysia elysian fields embalmer embassy ember embezzeler embiggening gun embiggening ray embryologist emcee emerald emergency blanket emergency exit emergency medical technician emergency room emergent emery emery board emery paper emiliana emiliana gavoni emily emily cox emo emo guy emp emp bomb emp grenade empanada empanizao empennage emperor emperor penguin empiricist employee employer employment office emporium empress empyrean emt emu emu apple emu tail emu wren emu-tail emu-wren emulator emuwren enamel encampment encephalographer encephalon enchanter enchantress enchilada enchiridion enclave enclosure encyclopedia endive endocardium endocrinologist endomorph endoscope endosulfan endrin enemy enemy fighter enemy fighter jet energumen energy bar energy drink enflurane engagement ring engine engineer engineering paper english barn english bulldog english cocker spaniel english horn english muffin english pointer english setter english springer spaniel english teacher engraver enjera enset ensete enshrinement enstatite entablement entanglement entertainer entertainment entertainment center entertainment centre entertainment park entomologist entophyte entrance entrance canopy entrance hall entrance way entrepreneur entresol envelope environment environment suit environmental scientist environmentalist environs envoy enxabeque eohippus eomuk eotyrannus epazote ephyna epic fail epichlorohydrin epidemiologist epistemologist epoxy eqalussuaq equalizer equid equine equine slipper equipment er eraser erato erbium eremomela ergonomist ergot erhu eric baudour eric boughton erica sabatello erica tringali erkuai ermelin ermine ern erne eros erpornis eruca erxian escalator escalope escape hatch escape pod escapee escaper escapeway escargot escarpment eschallot eschalotte escolar escomite escomite bean escort carrier escritoire espadrilles esplanade espresso espresso machine espresso pot essay establishment estate estate agent estate car estazolam esthetician estrella estuary et cetera etagere etc etcher eternal home eternal rest ethane ethanethiol ethanol ethanolamine ether ethicist ethinyloestradiol ethion ethnoastronomist ethnobotonist ethnologist ethologist ethyl acetate ethyl acrylate ethyl alcohol ethyl amyl ketone ethyl benzene ethyl bromide ethyl butyl ketone ethyl chloride ethyl ether ethyl formate ethyl silicate ethylamine ethylene ethylene chlorohydrin ethylene dibromide ethylene dichloride ethylene glycol ethylene glycol dinitrate ethylene oxide ethylene thiourea ethylenediamine ethylenimine ethylidene chloride ethylidene norbornene ethylmorpholine etima nut eton mess ettin etui etymologist eucalyptus eucalyptus tree eugenicist eulachon euoplocephalus euphonia euphonium euphoniumist euro sham eurohound european burmese european burmese cat european sham europium euryalida euterpe evangelist evaporative cooler eve evelynae even-toed ungulate evening dress evening gown evening wear event horizon everglade evergreen everlasting fire evidence evil genius evil knight evolutionary biologist evolutionist ewa ewa ewe ewer exam exam gown examinee examiner excalibur excavation excavator exchequer exciton executioner executive executive assistant exercise ball exercise bike exercise cycle exercise machine exercise room exercise station exhibit archive exhibition existentialist exit exit sign exomis exophthalmometer exoplanet exorcist exoskeleton experientialist experimental animal experimental subject experimentalist experimenter expert exploding barrel explorer explosive explosive d explosives expressman expressway extender extension extension cable extension cord extension ladder extension lead exterior door exterminator extinguisher extortionist extra extra terrestrial extrasolar planet extrovert extrudable explosives
i dont know bye :*