He PH PH. Ha 9 H-N Hc-c- Hc compound p

None

Ir spectrum for cyclohexanol and the peaks on the graph identified with the board,strong,weak, and the groups

Figure 3-9. 100 FUNSHINE 4800 001 Linti 4000 100 4900 3000 3000 3000 B 2008 2008 C 2008 HAVENUMER NAVENURIER-) NAVENUTEERIT CUST 1300 1900 1000 1000 1000 500 500

Can you please help me with this ochem question?

how does the chemical shift change when a carbon is connected to an electronegative atom via double bond compared to a single bond? Is the carbon signal for a carbon in a double bond with oxygen downfield or upfield?

fa) In the 400 MHz spectrum of a certain , separated by 4 ppm. The observed compound, there separated by 4 ppm. The observed coupling constant is 7 Hz. 6) What is this separation expressed in are two doublets Hz? f) In a 600-MHz instrument, what is the separation in Hz and in ppm?

Solution please, asked two times before but getting wrong answer. Please need correct, otherwise will report.

See attached picture.   Question.) Below is the NMR spectra and molecular formula for a molecule. Draw the complete structure in the box to the right below. All the atoms in each molecule are closed shell (octets) and uncharged. Lack of IR data does not mean that a specific functional group is not present in the molecule.

QUESTION #1 PROPOSE ANSWER FOR THE FOLLOWING SPECTRA ? AND JUSTIFY YOUR ANSWER