Is that the question orr......?
Hi, you have not provided structure of the aldehyde and alkoxide ion.
Therefore i'll show a mechanism corresponding to the proton transfer by considering a simple example.
Explanation: For an example, let's consider that proton transfer is taking place between a simple aldehyde e.g. acetaldehyde and a simple alkoxide base e.g. methoxide.
The hydrogen atom attached to the carbon atom adjacent to aldehyde group are most acidic. Hence they are removed by alkoxide preferably.
After removal of proton from aldehyde, a carbanion is generated. As it is a conjugated carbanion therefore the negative charge on carbon atom can conjugate through the carbonyl group to form an enolate which is another canonical form of the carbanion.
All the structures are shown below.
Answer:
A. 2NO + O2 -> 2NO2
B. 4Co + 3O2 -> 2Co2O3
C. 2Al + 3Cl2 -> Al2Cl6
D. 2C2H6 + 7O2 -> 4CO2 + 6H2O
E. TiCl4 + 4Na -> Ti + 4NaCl
Answer:
5.0 38 84.0 749.7 528.0 729.0 738.9 739.0
when heat gained = heat lost
when AL is lost heat and water gain heat
∴ (M*C*ΔT)AL = (M*C*ΔT) water
when M(Al) is the mass of Al= 225g
C(Al) is the specific heat of Al = 0.9
ΔT(Al) = (125.5 - Tf)
and Mw is mass of water = 500g
Cw is the specific heat of water = 4.81
ΔT = (Tf - 22.5)
so by substitution:
∴225* 0.9 * ( 125.5 - Tf) = 500 * 4.81 * (Tf-22.5)
∴Tf = 30.5 °C