Ha HaHaylaHoHo.HaHoHaНа НаCompund BTable 02: Predicted NMR peak assignments data for compoundВPredictedPredictedPredictedType of chemical Chemical shift multiplication/splittingvalue (ppm)integrationPeakenvironmentpatternAssignmentH,H,H. Complete the following NMR peak assignment tables. Predictthe chemical shifts, the splitting (multiplicity) pattern, andintegration for compound A - D. The chemical environments ofdifferent Hs in each molecule are labeled and assigned.Use the H-NMR peak reference chart to predict the correctchemical shift values.First two rows in table 01 is done for you as an example.HoHeHcHoHoHaНаHeHaHaCompund ATable 01: Predicted NMR peak assignments data for compoundAPredictedPredictedType of chemical Chemical shift multiplication/splittingvalue (ppm)PredictedPeakintegrationAssignmentenvironmentpattern3H0.5 – 1.5Triplet (t)H,C-CH32H3.5 – 4.5Quartet (q)H,H-C-OH.H.H,

Multiplicity of a proton is given by n+1 Where n = no of protons attached to the adjacent carbon

Answered: Complete the following NMR peak…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL3: Carbon (13c) Nmr Spectroscopy

Section: Chapter Questions

Problem 11E

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