Chemistry, 13.03.2021 01:00 lanettejohnson355

Consider the given 1H NMR spectrum, including TMS as reference, of a compound with a formula of C 9 H 11 B r O . Proton NMR spectrum with single TMS peak at 0 ppm, quintet centered around 2 ppm, a triplet at 3.15 ppm, a triplet at 3.65 ppm, two complex peaks around 7 ppm, and a triplet at 7.3 ppm. A closer view of the upfield signals is also available. Close up view of the proton NMR clearly showing quintet near 2 ppm, triplet at 3.15 ppm, and triplet at 3.65 ppm. What is the structure of the compound

Answers: 1

Show answers

Other questions on the subject: Chemistry

Chemistry, 21.06.2019 23:30, hellokitty1647

For the following dehydrohalogenation (e2) reaction, draw the zaitsev product(s) resulting from elimination involving c3â€“c4 (i. e., the carbon atoms depicted with stereobonds). show the product stereochemistry clearly. if there is more than one organic product, both products may be drawn in the same box. ignore elimination involving c3 or c4 and any carbon atom other than c4 or c3.

Answers: 3

continue

Chemistry, 22.06.2019 13:30, makenziehook8

Which is true of a liquid? it has a definite volume but not a definite mass. it has a definite mass but not a definite volume. it has a definite volume but not a definite shape. it has a definite shape but not a definite volume.

Answers: 2

continue

Chemistry, 22.06.2019 19:30, 2020sanchezyiczela

Draw the lewis structure for the trisulfur s3 molecule. be sure to include all resonance structures that satisfy the octet rule.

Answers: 3

continue

Chemistry, 22.06.2019 20:00, Ivy2k

Which of the following would not diffuse through the plasma membrane by means of simple diffusion? 1 oxygen 2 glucose 3 a steroid hormone 4 a lipid soluble vitamin

Answers: 3

continue

You know the right answer?

Consider the given 1H NMR spectrum, including TMS as reference, of a compound with a formula of C 9...