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AP®︎/College Chemistry
Course: AP®︎/College Chemistry > Unit 6
Lesson 1: Endothermic and exothermic processesEndothermic and exothermic processes
The first law of thermodynamics relates the change in the internal energy of a system (ΔE) to the heat transferred (q) and the work done (w). At constant pressure, q is equal to the change in enthalpy (ΔH) for a process. If ΔH is positive, the process absorbs heat from the surroundings and is said to be endothermic. If ΔH is negative, the process releases heat to the surroundings and is said to be exothermic. Phase changes, chemical reactions, and the formation of solutions are all examples of endothermic and exothermic processes. Created by Jay.
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- Are "q" and "w" defined based on how useful the energy transfer is to humans? For example, what sets work done by a system apart from heat transferred?
Can heat transferred be considered work?(5 votes) - At 7:72, how can a system absorb heat/energy from the surroundings, yet feel cold? Does it have something to do with forming/breaking chemical bonds or...(1 vote)
- If you're handling something undergoing an endothermic reaction it would feel cold to yourself because the reaction is drawing heat from the surroundings; in this case you. A lack of heat is interpreted by our bodies as being cold.
Hope that helps.(4 votes)
- I swear I've seen the exact opposite convention for work used...(1 vote)
- Yes, it is very much possible you have seen the exact opposite convention used. This is explained in further detail in the Khan Academy article on first law thermo:
"We have to be very careful with the first law. About half of textbooks, teachers, and professors write the first law of thermodynamics as ΔU=Q+W and the other half write it as ΔU=Q-W.
Both equations are correct, and they say the same thing. The reason for the difference is that in the formula ΔU=Q+W, we are assuming that W represents the work done on the system, and when we use ΔU=Q-W, we are assuming that W represents the work done by the system.
The two different equations are equivalent since,
W(on gas) = -W(by gas)"
https://www.khanacademy.org/science/ap-physics-2/ap-thermodynamics/ap-laws-of-thermodynamics/a/what-is-the-first-law-of-thermodynamics?modal=1(2 votes)
- At, Jay states how the system does 2 kJ of work on the surroundings. This confuses me because we assume an open container and constant pressure. If 2 kJ of work is applied on the surroundings, the container, doesn't that mean pressure changes? 4:39(1 vote)
- With an open container, the reaction is mostly going to doing work to the air surrounding the container (the air still being part of the surroundings). This will affect the air pressure of the room very slightly. But the pressure change of a chemical reaction on atmospheric pressure is so insignificant that we can still assume a constant air pressure in the surroundings.
Hope that helps.(2 votes)
- I'm not sure if this is the best place to ask, but what is enthalpy exactly? Thus far, I have come across two definitions: 1) the total heat content of a system 2) the change in heat content during a reaction. Are both of these correct? If so, going off of the former definition, since enthalpy is impossible to calculate, how do we know that certain systems have more than others? If we raise both a cube of ice and a glass of water in isolated systems by the same temperature, their change in enthalpies, or just enthalpies I suppose, would be the same, is this correct?(1 vote)
- Enthalpy is formally defined as the sum of a system’s internal energy and the product of its pressure and volume.
Or: H = E + PV, where H is enthalpy, E is internal energy, P is pressure, and V is volume.
Internal energy is the sum of heat and work from the first law of thermodynamics, while the pressure-volume term expresses the work required to establish the system’s physical surroundings, or to make room for it by displacing its surroundings. Like internal energy, it’s difficult to measure the absolute amount of enthalpy in a system so instead we measure the change in enthalpy from one state to another. Additionally by making the assumption that external pressure is constant we can do some algebra to find that the change in enthalpy is equal to the heat exchanged by the system and the surroundings. We can make the constant pressure assumption because most chemical reactions occur in open containers which do not significantly alter atmospheric pressure.
So: ΔH = q, where q is heat.
So in the vast majority of chemistry situations, enthalpy is measuring the amount of heat released or absorbed by the chemicals over the course of a reaction.
Hope that helps.(2 votes)
- And I wonder How the tutor got 2044?
And also how to deal this with equations(1 vote)- For your first question, that -2044 kJ value was provided in the question.
Your second question is too vague to answer, you need to specify more so.(1 vote)
- kind of a confusing explanation. so does q represent only heat? When you say 6000 J are flowing into the system do you mean that the piston is being force down compressing the He gas? how do you know the reaction is carried out by constant external pressure at? 5:00(1 vote)
- Yes, q is the usual variable used in these kind of thermodynamic problems. Heat is the transfer of energy, specifically thermal energy or the energy associated with temperature, from one object to another.
When 6000 J of heat is being added to the container, we are supplying 6000 J of thermal energy to the container. Pushing down on the piston would be us doing work on the container (positive work), which isn’t what is happening. Instead the 6000 J of heat is expanding the volume of the gas causing it to push back on the piston and do work on the surroundings (negative work).
Jay says the reaction is performed in an open container at. If the container is open then the external pressure is atmospheric temperature which is not changed significantly from a single chemical reaction’s negative work and can be assumed to be constant. 4:11
Hope that helps.(1 vote)
Video transcript
- [Educator] Before we get into the terms, endo and exothermic, We need to look at some
other thermodynamics terms that are used. For example, system. The system refers to
the part of the universe that we are studying. For our example, we're going
to consider a monatomic gas. Let's say we have some helium
particles in a container. And the helium gas represents our system. The surroundings are everything
else in the universe. So that would include this piston here and the cylinder in which the gas is in. And the universe consists
of both the system and the surroundings. Next, let's look at the
first law of thermodynamics which can be summarized by writing delta E is equal to Q plus W. Delta E is the change
in the internal energy of the system. And the internal energy refers to the sum of all the kinetic and potential energies of the components of the system. Since we have a monatomic
gas for our system, we only have kinetic energy. So if you could imagine
adding up the kinetic energy for each particle, the sum of those kinetic
energies for this example would be equal to the internal energy of the system. Q refers to the heat that's transferred from the system. So it's either transferred
to or from the system. And W refers to the work done on or by the system. Let's look at the sign conventions for the first law of thermodynamics. When we think about Q; when heat flows into the
system from the surroundings, we say that Q is positive. When heat flows out of the system and into the surroundings, we say that Q is negative. For work, when work is done on the system by the surroundings, the work is positive. But if work is done by the system on the surroundings, work is negative. It's very useful to think
about internal energy like a bank account. So if Q is positive and work is positive, that's like money coming
into your bank account. But if Q is negative or the work is negative, that's like money leaving
your bank account. Let's look at an example of
the first law of thermodynamics using our sample of helium that's in a cylinder with a movable piston. So let's say that 6,000 joules of energy. So 6,000 joules flows from the
surroundings into the system. And that heats up our helium particles, which then expand and push the piston up. So the piston gets pushed up, which is the system doing
work on the surroundings. And let's say that, that's 2000 joules of work done by the system on the surroundings. Using our assigned conventions, since heat flowed into the
system from the surroundings, that's a positive value for Q. And since the work was done by the system on the surroundings, that's a negative for the work done. So we can go ahead and plug in to the first law of thermodynamics. The heat transferred is
positive 6,000 joules and the work done as negative 2000 joules, therefore delta E or the change in the
internal energy is equal to positive 4,000 joules. Thinking about internal
energy like our bank account, we've gained 4,000 joules. So that could be like gaining $4,000. Since the system has gained 4,000 joules, that must mean the surroundings
has lost 4,000 joules. But since energy is conserved, the total energy of the
universe remains constant. Let's apply the first
law of thermodynamics to the combustion of propane and an open container
at constant pressure. For the combustion of propane, the reactants and products for the combustion reaction are considered to be the system, and everything else is the surroundings. So this combustion reaction
gives off 2,044 kilojoules of energy. So that's the heat that's
transferred from the system to the surroundings. The system also does
two kilojoules of work on the surroundings. So by convention, we make that negative. To find the change in the
internal energy of the system, we add Q plus W and get negative 2,046 kilojoules. Since this reaction was carried out under constant external pressure, we can write Q sub P here. So Q sub P is the heat that's transferred at constant pressure, and that is equal to the
change in the enthalpy, which is symbolized by delta H. So the change in enthalpy is the heat that's transferred at constant pressure. So the change in enthalpy for the combustion of propane is equal to negative 2,044 kilojoules. And notice how the change
in enthalpy is almost the same value as the change
in the internal energy. So the work done by the
system is a very small amount in this case, and that's usually the case. And since most chemical reactions are done under constant pressure, chemists care more about
the change in the enthalpy than they do about the change
in the internal energy. When delta H is negative, we call that an exothermic process. So the combustion of propane
is an exothermic reaction. An endothermic process is
where heat is transferred from the surroundings to the systems. So the system has gained
heat from the surroundings. The change in enthalpy, delta H is positive for
an endothermic process. An example could be melting an ice cube. If heat flows from the
system to the surroundings, the system has released
heat to the surroundings, and the change in enthalpy, delta H is negative. And we call this an exothermic process. And we already saw an example of that. The combustion of propane
is an exothermic reaction. So a phase change could be an endo or an exothermic process. A chemical reaction could also be an endo or an exothermic process. And even the formation of a
solution could be classified as an endo or an exothermic process. Let's think about making a solution. So let's say that we have a beaker and we have it full of water, and we take a solid and we dissolve the solid in the water to form a solution. If the dissolution process
is an exothermic process, that means the system releases heat to the surroundings. And since the beaker is
part of the surroundings, if we were to put our hand on the beaker and the beaker feels hot, we know that the disillusion of this particular solid
is an exothermic process. If we do the same thing
with another solid; so we dissolve this solid in water to form a solution. And we put our hand on the beaker, and this time the beaker feels cold. The reason the beaker feels cold is because energy was transferred
from their surroundings to the system. And so, the surroundings lost energy. And so, therefore we
can say the dissolution of this particular solid
was an endothermic process.