Johnny010
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Hello there. I am a 2nd year uni student studying chemistry. I have a paper in a few weeks on the foundations of physical chemistry.
I am having a problem with some quetions and would appreciate any help. Thank you to any who help.
1.Can the expectation value of the rotational angular momentum of a diatomic molecule
be used to predict what value will be obtained experimentally if the rotational angular
momentum of a single molecule is measure only once? Justify.
My answer:
The measurement of the observable <L> must be an eigenvalue to L(operator).
L(operator)fn(x)=Lnfn(x) n=1,2,3...
If the system is in an eigenstate of L(operator), the result gained must be of the observable L, that can only be of the particular eigenvalue characteristic of that eigenstate:
say Ψ(x)=f7(x)
then L=L7
Whereas if the system is not an eigenstate of L, the result of one measurement of a single diatomic can be in anyone eigenstate of L(operator) but will be completely unpredictable:
Ψ(x)≠fn(x)
The eigenvalue is therefore completely unpredictable.
The expectation value <L> would be given by:
Integration over all space of the wavefunction(in all co-ordinates)*L(operator) d(all co-ordinates).
Therefore <L> and the single measurement are unlikely to be the same.
I am having a problem with some quetions and would appreciate any help. Thank you to any who help.
1.Can the expectation value of the rotational angular momentum of a diatomic molecule
be used to predict what value will be obtained experimentally if the rotational angular
momentum of a single molecule is measure only once? Justify.
My answer:
The measurement of the observable <L> must be an eigenvalue to L(operator).
L(operator)fn(x)=Lnfn(x) n=1,2,3...
If the system is in an eigenstate of L(operator), the result gained must be of the observable L, that can only be of the particular eigenvalue characteristic of that eigenstate:
say Ψ(x)=f7(x)
then L=L7
Whereas if the system is not an eigenstate of L, the result of one measurement of a single diatomic can be in anyone eigenstate of L(operator) but will be completely unpredictable:
Ψ(x)≠fn(x)
The eigenvalue is therefore completely unpredictable.
The expectation value <L> would be given by:
Integration over all space of the wavefunction(in all co-ordinates)*L(operator) d(all co-ordinates).
Therefore <L> and the single measurement are unlikely to be the same.