explain how alkene/aromatic C-H stretches are distinguishable from alkane C-H stretches.

explain how alkene/aromatic C-H stretches are distinguishable from alkane C-H stretches. DO the C-H stretch peaks in the IR spectra of triphenylmethanol, bromobenzene, and benophenone occur in the expected alkene/aromatic C-H stretching region?

tri-phenyl methanol has more steric effect so it is expected to have some what higher valuethan the normal [ Ph2C – gr. Has +ve inductive effect So the ortho carbon charge density is not...