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Properties of some common solvents.

solvent
acetone chloroform diethyl ether ethanol (95%) ethyl acetate hexanes isopropanol methanol methylene chloride toluene water

formula
(CH3)2C=O CHCl3 (CH3CH2)20 CH3CH2OH CH3CO2CH2CH3 C6H14 CH3CHOHCH3 CH3OH CH2Cl2 C6H5CH3 H2O 56 61 35 78 77

bp (C)

density (g/mL)
0.8 1.5 0.7 0.8 0.9 0.7 0.8 0.8 1.3 0.9 1.0

hazards
ammable toxic highly ammable ammable ammable ammable ammable ammable, toxic toxic ammable

6769 82 65 41 111 100

Properties of some common acids and bases. compound


acetic acid, conc., 99.8% sulfuric acid, conc., 96% phosphoric acid, conc., 85% nitric acid, conc., 70% hydrochloric acid, conc., 37% ammonium hydroxide, conc., 29%

formula
CH3CO2H H2SO4 H3PO4 HNO3 HCl NH4OH

MW of pure compound
60.05 98.08 98.00 63.02 36.47 35.05

normality
17.4 36 14.7 17 12 14.8

density (g/ mL)


1.05 1.84 1.69 1.42 1.19 0.90

Some properties of salts/salt solutions used in organic chemistry. name


sodium bicarbonate sodium carbonate sodium chloride

formula
NaHCO3 Na2CO3 NaCl

MW
84.00 106.00 58.45

solubility
1 part in 10 parts water at 25 1 part in 3.5 parts water at 25 1 gram dissolves in 2.8 mL of water at 25

miscellaneous
pH of 0.1 M aq. solution = 8.3; density is about 1 Density is about 1 Density of saturated solution = 1.202

Chromatography solvents eluting order. hexanes increasing polarity (more powerful eluters) toluene methylene chloride diethyl ether ethyl acetate acetone methanol, ethanol acetic acid

Usual eluting order of organic compounds. saturated hydrocarbons unsaturated hydrocarbons more polar (stronger bonding) ethers esters halides ketones aldehydes amines alcohols acids and bases

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