Question 1  How many signals would you expect to see in the proton NMR spectrum of the following compound?  Question 2  The protons indicated in the structure below would show up as a __________ in a proton NMR spectrum.  Answer A.singletB.doubletC.tripletD.quartetE.septet 1 points   Question 3  Which structure of molecular formula, C4H8Cl2, fits the proton NMR spectrum shown below?  Answer A.B.C.D.1 points   Question 4  Which compound has a proton NMR spectrum consisting of the following peaks: 0.9 (6H, doublet), 1.0 (3H, triplet), 2.2 (2H, quartet), and 4.0 (1H, septet)? Notation: Chemical shift values are listed first in ppm. The absolute number of hydrogens and their multiplicities are given in parentheses. Hint: A few of the structures might fit the splitting patterns, so you will also need to consider the chemical shift values. Answer A.B.C.D.1 points   Question 5  Which of the following protons gives an NMR signal with the highest chemical shift value (farthest downfield)?  Answer A.1B.2C.3D.4E.51 points   Question 6  Which structure of molecular formula, C7H14O, fits the proton NMR spectrum shown below?  Answer A.B.C.D.E.1 points   Question 7  How many of the following compounds are aromatic?  Answer 2 points   Question 8  Which of the following is the electrophile that attacks the aromatic ring during sulfonation? Answer A.HSO3+B.SO2+C.HSO3-D.H2SO4E.HSO4-1 points   Question 9  What is the major organic product of the Friedel-Crafts alkylation reaction between benzene and isobutyl chloride in the presence of AlCl3? Answer A.tert-butylbenzeneB.isobutylbenzeneC.n-butylbenzeneD.chlorobenzeneE.sec-butylbenzene
Already registered? Login
Not Account? Sign up
Enter your email address to reset your password
Back to Login? Click here