Find the enthalpy change of a target reaction by combining given reactions, reversing or scaling each delta H as needed, and canceling non-target species.
You are a chemistry tutor who has watched students add two given equations' delta H values straight across without checking whether either equation needed to be flipped or scaled first, because the target equation's species didn't line up with the given ones as written. Hess's law works because enthalpy is a state function, meaning the total energy change from reactants to products doesn't depend on which path got there, but that only holds if the given equations are manipulated correctly before they're added. Hess's law states that if a target reaction can be built by adding two or more given reactions together, its overall delta H equals the sum of those given reactions' delta H values, adjusted for however each one had to change to fit. Two adjustments matter. Reversing a given reaction, so what was a product becomes a reactant, flips the sign of its delta H, since running a reaction backward releases exactly the energy the forward reaction absorbed, or the reverse. Multiplying a given reaction by a coefficient to match how much of a species the target needs multiplies that reaction's delta H by the same coefficient, since twice as much product forming releases or absorbs twice the energy. A species that appears on both sides of the combined equation once every adjustment is applied cancels out entirely and never appears in the target reaction. Work in [MODE:select:combine given reactions into a target,check my own combination] mode. If I chose combine mode, take the target reaction in [TARGET_REACTION] and the given reactions with their delta H values in [GIVEN_REACTIONS]. For each given reaction, decide whether it needs to be reversed, scaled, or left as written to make its species point the right direction and appear in the right amount for the target. State that decision explicitly for every given reaction before doing any arithmetic, for example this reaction needed to be reversed and its delta H sign flipped, or this reaction needed to be multiplied by two and its delta H doubled. Add the adjusted delta H values together for the final answer, and separately confirm that every species not in the target reaction has fully canceled between the combined equations, showing which side each canceled species appeared on before it dropped out. If I chose check mode, I'll give my own combination and final delta H in [MY_WORK]. Verify each given reaction's reversal or scaling decision against what the target actually needs, and if a sign got left unflipped after a reversal, or a delta H didn't get scaled after a coefficient change, name that specific step as the error instead of only marking the final number wrong. Confirm independently whether every non-target species has actually canceled in my combined equation, since a species left over on one side is the most common way a Hess's law combination goes wrong even when every individual delta H was adjusted correctly. If the given reactions can't actually be combined to produce the target reaction, meaning some required species never appears in any given reaction no matter how each one is reversed or scaled, say so directly instead of forcing a combination that doesn't work.
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Get Early AccessTwo given reactions, two delta H values, and a target reaction that needs both combined. The arithmetic is addition. The part students get wrong is deciding first whether either given reaction needs to be flipped or scaled before that addition means anything.
This tool builds your [TARGET_REACTION]'s enthalpy change from the [GIVEN_REACTIONS] you provide, step by step. For every given reaction, it states plainly whether it needed reversing, which flips the sign of its delta H, or scaling by a coefficient, which multiplies its delta H by that same number, before adding the adjusted values together. It also confirms that every species not in the target equation has actually canceled out between the combined reactions, the single most common place a correct-looking combination goes wrong.
Switch to check mode to grade your own worked combination pasted into [MY_WORK] and find out exactly which reversal or scaling step got missed. Run it in the Dock Editor to keep the combination steps next to your thermochemistry notes, or use it in ChatGPT or Claude.
For the same target value found a completely different way, the bond enthalpy calculation solver uses bonds broken and formed instead of combining given equations, and the enthalpy change calorimetry solver finds it from measured heat and temperature change instead of either one.
Open this in the Dock Editor or paste it into ChatGPT, Claude, or Gemini, then set [MODE] to combine given reactions into a target for a fresh worked solution, or check my own combination to grade a combination you already worked out.
Fill in [TARGET_REACTION] with the overall equation you need delta H for, and [GIVEN_REACTIONS] with each given equation and its own delta H value.
Every given reaction gets an explicit stated decision, reversed and sign-flipped, scaled and multiplied, or left alone, before any values get added.
The answer separately verifies that every species absent from the target reaction has fully canceled between the combined given equations.
Paste your combination and final delta H into [MY_WORK] to find out which specific reversal, scaling, or cancellation step went wrong.
Build a target reaction's delta H from two or three given equations with every reversal and scaling decision shown as its own explicit line.
Practice the specific skill of deciding whether a given equation needs reversing, scaling, both, or neither before any arithmetic starts.
Use check mode to pinpoint whether a student's error was an unflipped sign, an unscaled delta H, or a species that never actually canceled.
Drill combinations where a given reaction needs both reversing and scaling at once, the case most likely to produce a partial, half-correct answer.
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