Yes it is somehow;the strategy for estimating reaction enthalpies is a straightforward application of Hess's law:
As we know Hess's law states that if a rxn is carried out in a series of steps, delta H for the reaction will equal the sum of the enthalpy changes for the individual steps.
And he stated that all chemical reactions can be broken down into formation reactions( Enthalpies of formation), so basically all chemical reactions can be broken down to steps that their enthalpies are enthalpies of formation.When we do(by using hess law), we obtain the general result that the standard heat of reaction is the sum of the standard heats of formation of the products minus the standard heats of formation of the reactants. ( I don wanna make this more complicated by explaining why you put minus in the formula)
Also for calculating the enthalpies of reactions by using bond enthalpies, we again used the Hess' law:
We can imagine that all reactions occur in 2 steps: 1) first step, breaking all bonds. 2) second step, formation of bond
So the enthalpy of the reaction is estimated as the sum of the bond enthalpies of the bonds broken(reactants), minus the sum of the bond enthalpies of the new bonds formed(products), and keep in mind we put minus because, formation of bond is an exothermic reaction.So here, it's important to put (-) before the bond enthalpies of products, because the new bonds only form in the products. And bonds only break in the reactants( endothermic). In your sln manual, they wrote it
-(bonds formed in products)+ (bonds broken in reactants) instead of (bonds broken)-(bonds formed), same thing.