Since Enthalpy $(H)$ is a state function, it can be expressed as a function of either of the two variables of $P,\,V,\,T\,.$
So, consider enthalpy as a function of $T$ and $P\,.$
So, its differential can be written as
$$\mathrm dH = \left(\frac{\partial H}{\partial T}\right)_P ~\mathrm dT + \left(\frac{\partial H}{\partial P}\right)_T~\mathrm dP\tag I$$
From the First Law and assuming non-compression work is zero, we get
$$\mathrm dH= đq + V~\mathrm dP\tag{II}$$
Now,
\begin{align}\mathrm dS &= \frac{đq}{T}\\ \implies \mathrm dS &= \frac{(\mathrm dH- V~\mathrm dP)}{T}~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~[\mathrm{Using~~ II}]\\ \implies \mathrm dS &= \frac1T\left(\frac{\partial H}{\partial T}\right)_P~\mathrm dT + \frac1T\left[\left(\frac{\partial H}{\partial P}\right)_T- V\right]~\mathrm dP~~~~~~~[\mathrm{Using~~ I}]\tag{III}\end{align}
Also, $$\mathrm dS= \left(\frac{\partial S}{\partial T}\right)_P~\mathrm dT + \left(\frac{\partial S}{\partial P}\right)_T~\mathrm dP\tag{IV}$$
Comparing $\rm (III)$ and $\mathrm{ (IV)}$ we get
\begin{align}\left(\frac{\partial S}{\partial T}\right)_P&=\frac1T\left(\frac{\partial H}{\partial T}\right)_P\\\implies \left(\frac{\partial S}{\partial T}\right)_P&= \frac{C_p}T\,. \tag{V} \end{align}
"[…]Since the temperature change accompanying a chemical reaction does not result from heat transfer via conduction, convection or radiation […]"
I think there's some confusion here. It is confusing to ascribe the temperature change to a flow of heat. The point is, surely, that in exothermic reactions heat escapes from the system of reactants, usually by conduction through the walls of the conducting vessel. The heat flow takes place because, due to the reaction, the temperature of the reactants/products becomes greater than that of the vessel and its surroundings.
In thermodynamics, heat is not a property of a system, but is energy in transit to or from the system. However enthalpy is a property of the system. We can equate the enthalpy change to the heat flow only when the pressure is constant.
Best Answer
For a reversible adiabatic (constant entropy) process for an ideal gas, pressure varies with volume according to
$$PV^{\gamma}=C$$
Where $C$ is a constant. So pressure cannot be constant.
A constant pressure adiabatic process is an irreversible process. See:
https://physics.stackexchange.com/questions/577884/is-a-constant-pressure-adiabatic-irreversible-expansion-possible#:~:text=That%2C%20of%20course%2C%20can',external%20pressure%20expansion%20or%20contraction.
So a constant pressure adiabatic process generates entropy, i.e., $dS>0$, in spite of the fact that $Q=0$.
Hope this helps.