Its 16.667% or 16 1/3%
Expected successes= Theoretical Probability · Trials P(event) = Number of possible out comes divided by total number of possible
The formula is:1 pint = 16 ounces
4 * 2 = 8 1 * 16 = 16 16 + 8 = 24
The formula for multiplicatin and addition is that you multiply th area and you add the perimiter for example if you had a sqare and each side were 4in. and inside had 16 blocks in there it would be 4 times 4 and you wold get 16, so 16+16=32 so thats the answer.And thats how you use the formula.
There is no "limit" set by the USP, it depends on the molecules and what is reasonable. For example in HPLC, 2000 plates is typically what you would like to shoot for but if its a compound with low sensitivity and you need to see low levels you might inject more compound which would increase sensitivity but also probably affect peak shape and thus theoretical plates. The answer is it depends
A higher number of theoretical plates indicates better separation efficiency in chromatography. Each theoretical plate represents a stage in the column where equilibration between the stationary and mobile phases occurs, leading to increased resolution of components in the sample. More theoretical plates result in better separation and sharper peaks, indicating higher efficiency in the chromatographic process.
Percent Error = {Absolute value (Experimental value - Theoretical Value) / Theoretical Value }*100
The formula for the electric field between two plates is E V/d, where E is the electric field strength, V is the voltage difference between the plates, and d is the distance between the plates.
To calculate the theoretical pH of a solution, you can use the formula pH -logH, where H represents the concentration of hydrogen ions in the solution. This concentration can be determined from the chemical equation of the reaction or by using the initial concentrations of the reactants. By plugging in the H value into the formula, you can find the theoretical pH of the solution.
Its 16.667% or 16 1/3%
A= 4 times the base of square mass
The formula for calculating the electric field between two parallel plates is E V/d, where E is the electric field strength, V is the potential difference between the plates, and d is the distance between the plates.
The formula for calculating the electric field strength between two plates is E V/d, where E is the electric field strength, V is the potential difference between the plates, and d is the distance between the plates.
16
The number of theoretical plates in a chromatography column is a measure of how "long" the column is - how well it separates. A "short" column will only separate large or heavy molecules, and the medium and light stuff is still mixed together in the last band. A "long" column will separate the little stuff better because there are more theorectical plates. Picture a stack of sieves with smaller and smaller holes as the column gets "longer" and you've got the idea. This "length" has virtually nothing to do with the physical length of the separating column. It is a function of the packing materials and solvents used during a separation.
Expected successes= Theoretical Probability · Trials P(event) = Number of possible out comes divided by total number of possible