Question
Explain # 7 compound name P-Chlorophenol
elaborate on What 7. NMR-both C13 and HI -Please include the spectra-Please each peak Why is it a singlet? Why is it downfield or upfield? What peak corresponds to what signal etc... Nuclear Magnetic Resonance (list all peaks) Protons Chemical Shift(ppm) Aromatic Multiplicity-1 Integration 6.9 3.5 NHz Conclusion Please show the name and the chemical structure (Lewis Structure) of the compound. Show how (chemical equation) it is synthesized and the mechanism (chemical equations with electron arrows). Uses of the compound and any problems, environmentally or health wise associated with the compound.
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C t H CA 8) rt h (B) There vett, vee different type)of pyotow present m กา 2 H 2ケ l H Avemodic (A) 1 O-H 2 downteeld to 9-2 pm ave to anis ohopic efect Hy Moosen C is attached ts move elecho nagedive ten 2 Ppm 3 C A 1 2.

In case of p-chlorophenol, there are three types of hydrogens are present which are shown by A, B and C. Hydrogen type A and B are aromatic hydrogen which are having chemical shift downfield due to anisotropy in benzene. This oppose the normal spin. In case of type A, hydrogens are close to highly electronegative Cl, thus more downfield is observed. In case of OH, the hydrogen attached to the more electronegative oxygen results into more chemical shift that is downfield.

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