Is hso3- acting as an oxidizing or reducing agent
In the experiment, sodium bisulfite solution is added at the end in order to destroy the unreacted bromine. What reaction is occurring here? Is HSO3- acting as an oxidizing or reducing agent? Write a balanced equation as part of your answer
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. a) Write the rate law for the reaction. b) What is the rate of reaction when [N2O5]= 0.0240 M? c) What happens to the rate when the concentration of N2O5 is doubled to 0.0480M?
Calculate the theoretical yield percentage of a reaction between sodium and water, if 25.0 g of sodium react with excess water and if 15.5 L of gaseous hydrogen are collected at NTP conditions.
calculate the number of grams of acetic acid per 10ml of the vinegar. Since vinegar has a density of about 1.00 gram/ml, 100 ml eighs about 100 g. thus this calculation also gives the percent by weight of acetic acid in the vinegar. compare with m
A small collection of dimes and quarters are submerged in 10.00 mL of water in a graduated cylinder causing the water level to rise to the 18.87 mL mark. What is the combined monetary value (in Can$) of those coins?
In the experiment, sodium bisulfite solution is added at the end in order to destroy the unreacted bromine. What reaction is occurring here? Is HSO3- acting as an oxidizing or reducing agent? Write a balanced equation as part of
You deposit $1,541 in a bank for 19 years. What is the amount you will have in the bank at the end of 19 years if interest of 4 % for first 5 years and interest of 8 % for the remaining years? Note: Do not put $ sign in your answer. Simply write t
A solution is initially 2.5 ? 10-3 M in Cu+ and 2.5 ? 10-3 in Pb 2+. Iodine ion is gradually added to the solution. Determine the concentrations of Cu+, Pb +2, and I- at the point of maximum separation.
A sample of molten iron occupies of a volume of 7.11 x 10-3 L. If the density of iron is 7.86 g/cm3, what is the mass of iron in grams in the sample?
What is the condensed structural formula for 2,2-dimethyl, 4-heptyne
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Permeability is a common bottleneck for PROTACs; however, for other drug types, how is it decided which parameter is the bottleneck?
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