[Cu(NH3)4]^+2 solutions exhibit a deep blue-violet color. How can you use spectrophotometry to confirm that this reaction has oc
2 answers:
Answer : Use of spectrophotometry to study the absorbance changes during the course of reaction which can confirm that tetraamine copper(II) sulfate is formed or not is by comparing the absorbance of the solution with the literature absorbance value of tetraamine copper(II) sulfate. After comparison if both are found to be almost similar then it can be confirmed that tetraamine copper(II) sulfate is the product formed.
The wavelength of is less than λ max for
because it absorbs in the range of shorter wavelength of yellow light. Therefore, the solution appears to be deep blue-violet color.
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Answer : The % of (+) limonene isomer = 79%
The % of (-) limonene isomer = 0%
The % of enantiomeric excess = 58%
Explanation : Enantiomeric excess (ee) is the measurement of purity used for chiral substances.
Given,
% of pure limonene enantiomer = The % of (+) limonene isomer = 79%
Therefore, The % of (-) limonene isomer = 0%
Formula used :
Where, ee → enantiomeric excess
Now, put all the values in above formula, we get the value of enantiomeric excess (ee).
= 58%
Answer:
Explanation:Since the compound X has no net-dipole moment so we can ascertain that this compound is not associated with any polarity.
hence the compound must be overall non-polar. The net dipole moment of compound is zero means that the vector sum of individual dipoles are zero and hence the two individual bond dipoles associated with C-Cl bond must be oriented in the opposite directions with respect to each other.]
So we can propose that compound X must be trans alkene as only in trans compounds the individual bond dipoles cancel each other.
If one isomer of the alkene is trans then the other two isomers may be cis .
Since the two alkenes give the same molecular formula on hydrogenation which means they are quite similar and only slightly different.
The two possibility of cis structures are possible:
in the first way it is possible the one carbon has two chlorine substituents and the carbon has two hydrogens.
Or the other way could be that two chlorine atoms are present on the two carbon atoms in cis manner that is on the same side and two hydrogens are also present on the different carbon atoms in the same manner.
Kindly refer the attachments for the structure of compounds:
