Conjugate base of Propanoic acid (
is propanoate where -COOH group gets converted to -CO
. The structure of conjugate base of Propanoic acid is shown in the diagram.
The
above which 90% of the compound will be in this conjugate base form can be determined using Henderson's equation as propanoic acid is weak acid and it can form buffer solution on reaction with strong base.
=
+ log
=4.9+log
=5.85
As 90% conjugate base is present, so propanoic acid present 10%.
Answer: Theoretical Yield = 0.2952 g
Percentage Yield = 75.3%
Explanation:
Calculation of limiting reactant:
n-trans-cinnamic acid moles = (142mg/1000) / 148.16 = 9.584*10⁻⁴ mol
pyridium tribromide moles = (412mg/1000) / 319.82= 1.288*10⁻³ mol
- n-trans-cinnamic acid is the limiting reactant
The molar ratio according to the equation mentioned is equals to 1:1
The brominated product moles is also = 9.584*10⁻⁴ mol
Theoretical yield = (9.584*10⁻⁴ mol) * (Mr of brominated product)
= (9.584*10⁻⁴ mol) * (307.97) = 0.2952 g
Percentage Yield is : Actual Yield / Theoretical Yield = 0.2223/0.2952
= 75.3%
We are given with
136 g P4
excess oxygen
The complete combustion reaction is
P4 + 5O2 => 2P2O5
Converting the amount of P4 to moles
136/123.9 = 1.098 moles
Using stoichiometry
moles P2O5 = 1.098 x 2 = 2.195 moles P2O5