For the reversible isothermal expansion from state I to II:
So, all options are correct for this expansion.
For the reversible adiabatic expansion from state II to III:
Option (C) does not follow the condition of decreasing enthalpy, so it is incorrect. Options (A), (B), and (D) all follow the conditions, so they are correct.
Therefore, correct graphical representations for the given conditions are (A), (B), and (D).
The enthalpy of combustion of methane is 890 kJ/mol. How much heat is released when 8 g of methane is burned completely? (Molar mass of CH\(_4\) = 16 g/mol)
Let $ S $ denote the locus of the point of intersection of the pair of lines $$ 4x - 3y = 12\alpha,\quad 4\alpha x + 3\alpha y = 12, $$ where $ \alpha $ varies over the set of non-zero real numbers. Let $ T $ be the tangent to $ S $ passing through the points $ (p, 0) $ and $ (0, q) $, $ q > 0 $, and parallel to the line $ 4x - \frac{3}{\sqrt{2}} y = 0 $.
Then the value of $ pq $ is
Enthalpy Change refers to the difference between the heat content of the initial and final state of the reaction. Change in enthalpy can prove to be of great importance to find whether the reaction is exothermic or endothermic.
dH = dU + d(PV)
The above equation can be written in the terms of initial and final states of the system which is defined below:
UF – UI = qP –p(VF – VI)
Or qP = (UF + pVF) – (UI + pVI)
Enthalpy (H) can be written as H= U + PV. Putting the value in the above equation, we obtained:
qP = HF – HI = ∆H
Hence, change in enthalpy ∆H = qP, referred to as the heat consumed at a constant pressure by the system. At constant pressure, we can also write,
∆H = ∆U + p∆V
To specify the standard enthalpy of any reaction, it is calculated when all the components participating in the reaction i.e., the reactants and the products are in their standard form. Therefore the standard enthalpy of reaction is the enthalpy change that occurs in a system when a matter is transformed by a chemical reaction under standard conditions.