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Consider the hypothetical reaction of A, which could yeild one or both of the two products B and C, depending on the reaction conditions. Whereas B has been determined to be the kinetic product, C has been determined to be the thermodynamic product. Complete potential energy diagrams for the formation of B and C by sketching the energy curve for each product.
Explain why light intensity is dependent on the distance the detector is from the light source. Describe the mathematical relationship. Explain why all comparative measurments for this experiment should be made with the optical cable the same dist..
The kinetic energy of the ejected electron is given by 1/2 mv2= h v -?. where m and v are the mass and velocity of the electron
how many grams of ch4 must be burned to release 490 kj of heat based on this thermochemical equationch4 2 o2 --gt co2
Compound A has the molecular formula C14H25Br and was obtained by reaction of sodium acetylide with 1,12-dibromododecane. On treatment of compound A with sodium amide
Carboxylic acids have higher than expected boiling points due to dimeric associations involving hydrogen bonding. The structure of 3-methylbutyric acid is shown below. Draw a second molecule of 3-methylbutyric acid
Give an example of a compound that exhibits ionic bonding and an example of a compound that exhibits a covalent bond.
1. calculate the volume of carbon dioxide at 273 k and 1.01 105 pa which would be produced when 1.25g of calcium
A gas has an initial volume of 2.75 L at temperature of 285 K. If the temperature changes to 380 K, what is the new volume of the gas if the pressure is unchanged?
What types differences in the H-NMR spectra of starting material and product do you expect to see camphor, borneol
Write the balanced equation for the reaction involved in the synthesis of acetanilide from aniline and acetic anhydride.
N2 +3H2= 3NH3 What is the limiting reactant/ maximum number of moles of NH3 formed from 2.0 moles of n2 and 2.0 moles of H2
Important information about Nitration, Explain why nitration of 1,4-dichloro-benzene yields the mononitro derivative while N,N'-diacetyl-1,4-phenylenediamine forms
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