Answer: option C. Copper (II) chloride
Explanation:
To name CuCl2, we need to know the oxidation state of Cu in the compound as chlorine always have oxidation on —1 in all its compound. The oxidation state of Cu can be calculated as follows:
Cu + 2Cl = 0 (since the compound has no charge)
Cl = —1
Cu + 2(—1) = 0
Cu —2 = 0
Collect like terms
Cu = 0 +2
Cu = +2
Therefore, the oxidation state of Cu in CuCl2 is +2.
The name of the compound will be copper(ii) chloride, since cupper has oxidation state +2 in the compound.
The atoms didn't change we only added 2 different ones together. 2nd one is right
Lithium is a good reducing agent because it is electropositive [it rapidly gains electrons]
fluorine is good oxidizing agent electronegative [it loses electrons fastly]
Answer:
The correct answer is 160.37 KJ/mol.
Explanation:
To find the activation energy in the given case, there is a need to use the Arrhenius equation, which is,
k = Ae^-Ea/RT
k1 = Ae^-Ea/RT1 and k2 = Ae^-Ea/RT2
k2/k1 = e^-Ea/R (1/T2-1/T1)
ln(k2/k1) = Ea/R (1/T1-1/T2)
The values of rate constant k1 and k2 are 3.61 * 10^-15 s^-1 and 8.66 * 10^-7 s^-1.
The temperatures T1 and T2 are 298 K and 425 K respectively.
Now by filling the values we get:
ln (8.66*10^-7/3.61*10^-15) = Ea/R (1/298-1/425)
19.29 = Ea/R * 0.001
Ea = 160.37 KJ/mol
Answer:
See explanation
Explanation:
A. Constitutional or structural isomers have the same molecular formula but different structural formulas.
B. Conformational isomers are compounds having the same atom to atom connectivity but differ by rotation about one or more single bonds.
C. Stereo isomers are compounds having the same molecular mass and atom to atom connectivity but different arrangement of atoms and groups in space.
I. Enantiomers are stereo isomers (optical isomers particularly) that are non-superimposable mirror images of each other.
II. Diasteromers are optical isomers that are not mirror images of each other.
Both diasteromers and enantiomers are types of optical isomers which in turn is one of the types of stereo isomers.
Stereo isomers differ from conformational isomers in that the arrangement of atoms in stereo isomers is permanent while conformational isomers results from free rotations in molecules about single bonds.
