
the way that you get 66 is by adding he atomic mass unit of each atom in the formula. so N2 is 14 + 14 H4 is 1 * 4 and 03 is 16 * 3
We are asked to provide an equation for the transformation of 2-phenylethanoic acid to 2-phenylethanol. This type of a reaction is converting a carboxylic acid to an alcohol, which is classified as a reduction reaction since we are decreasing the number of bonds to oxygen in the molecule. In order to reduce a carbonyl to an alcohol, we need a source of hydride, H⁻. Reducing the carboxylic acid once will convert it to the aldehyde. However, we need to reduce the functional group all the way down to an alcohol, which is another reduction step after aldehyde formation. Therefore, the hydride source of choice is lithium aluminum hydride, LiAlH₄.
A reaction scheme is provided to show the reaction of the reduction of carboxylic acid to alcohol. The first step is addition of lithium aluminum hydride which does the reduction, and the second step is a work-up of acid which protonates the alcohol to get the final product.
At STP, or standard temperature and pressure, 1 mol of any gas will take up 22.4 liters of space. Assuming STP, 4.5 moles of H2 will take up 100.8L.
By definition, Bronsted-Lowry acid is a proton donor in the acid-base neutralization reaction. When a weak acid like acetylsalicylic acid is reacted with water, the water here acts as the Bronsted-Lowry base. This is possible because water has properties of amphoterism - can act as an acid or base. In this case, acetylsalicylic acid would have to donate its H+ atom to water, so that it would yield a hydronium ion, H₃O⁺. The complete net ionic reaction is shown in the picture.
So, in the reaction, the products yield are the acetylsalicylate ion and the hydronium ion.