In 'x' mL 0.3 N HCl, the addition of 200 mL distilled water or addition of 100 mL 0.1 N NaOH, gives the same final acid strength. Determine 'x'.
Compound A treated with NaNH2 followed by CH3CH2Br gave compound B. Partial hydrogenation of compound B produced compound C, which on ozonolysis gave a carbonyl compound D, (C2H5O). Compound D did not respond to the iodoform test with I2/KI and NaOH. Find out the structures of A, B, C and D.
The bacterial growth follows the rate law, dN/dt = kN where k is a constant and 'N' is the number of bacteria cell at any time. If the population of bacteria (number of cell) is doubled in 5 min find the time in which the population will be eight times of the initial one?
As dN/dt = kN (It is a Ist order reaction)
Integrated rate equation for Ist order reaction
k = 2.303/t log N/No
when t = 5 min, N = 2No
k = 2.303/5 log 2No/No
or k = 2.303/5 log 2
for N = 8No , t = ?
t = 2.303/k log 8No/No
By putting the value of k
t = log 8No/N
or t = = 15 min
An organic compound with molecular formula C9H10O forms 2, 4-DNP derivative, reduces Tollen's reagent and undergoes Cannizaro reaction. On vigorous oxidation, it gives a dicarboxylic acid which is used in the preparation of terylene. Identify the organic compound.
Deep blue CuSO4.5H2O is converted to a bluish-white salt at 100oC. At 250oC and 750oC it is then transformed to white powder and black material respectively. Identify the salts.