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how would you synthesize 2-ethyl-1,3-hexanediol in the lab setting? starting from simple organic compounds such as benzene, toluene, benzaldehyde, acetophenone or molecules containing 6 carbons or less
A mixture of gases containing 21.0 g of N2, 106.5 g of Cl2, and 12.0 g of He at 14 oC is in a 50.0 L container. What is the partial pressure of N2.
Imagine that you have two iron blocks, one with a mass 226 g at a temperature of 46.0 oC, and another with a mass 380 g at a temperature of 134 oC. The two blocks are brought into contact with each other in an insulated container. What is the fina..
Important information about Chem problem, A 25 mL sample of .13M HCl is mixed with 15mL of .24M NaOH. The pH of the resulting solution will be nearest. The answer is 11.9
Find out the formula of the gas produced if Na 3 P(s) sodium phosphide, is reacted with H 2 O
A compound contains only carbon, hydrogen, nitrogen and oxygen. Combustion of 0.314 g of the compound produced 0.426 g CO2, and 0.0620 g H2O
Two compounds have the same empirical formula. One substance is a gas, the other is a viscous liquid. How is it possible for two substances with the same empirical formula to have markedly different properties?
the pressure of a sample of a 1000 mL sample of gas at 10.0C increases from 700 mm Hg to 900 mm Hg. If the volume is unchanged, what is the new temperature
If 7.63 of an unknown gas occupies 79.1mL at 25.02 degrees celcius and 7.55 atm of pressure, what is the molar mass of the gas? R=0.0821
Calculate the pH of 1.00 L of the buffer 1.01M CH3COONa/1.01M Ch3COOH before and after the addition of the following species. (Assume there is no change in volume). (a) pH of starting buffer:
The absence of an alkene C=C IR stretch is definitive evidence that a compound lacks an alkene functional group.
Find the pH of a solution prepared by dissolving all of the following compounds in one beaker and diluting to a volume of 1.00 L: 0.180 moles acetic acid (pKa=4.75), 0.180 mole sodium acetate
In Horner-Wadsworth-Emmons reaction, a 1,2-disubstituted alkene was produced in which the olefinic protons exhibited at vicinal coupling of 9.0 Hz in the 1H NMR. What is the stoichiometry of the double bond.
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