1. 1H NMR

2. Hexane (C6H14 ) 89.56 MHz (CDCl3) Assign. Shift (ppm) A 1.29 B 1.27
J(A,C) = 6.9 HZ.

3. Octane (C8H18) MHz (CDCl3)
Assign. Shift (ppm) A B

4. Isopentane (C5H12) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D
J(B,D)=7.3 HZ.
J(A,C)=6.6 HZ.
J(A,B)=6.6 HZ

5. 2-Propanol (C3H8O) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C

6. 3-Chloro-1-propanol (C3H7ClO) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D

7. Chloroethylene (C2H3Cl) 300 MHz (CCl4)
Assign. Shift (ppm) A B C
J(A,B)= Hz
J(A,C)= Hz
J(B,C)=14.46 Hz

8. Styrene (C8H8) 86.59 MHz (CDCl3)
Assign. Shift (ppm)
A to 7.10 B C D

9. p-Xylene (C8H10) 300 MHz (CDCl3)
Assign Shift (ppm) A B

10. 2-Bromo-p-xylene (C8H9Br) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D E

11. Ethyl acetate (C4H8O2) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C
J(A,C)=7.1HZ.

12. Butyraldehyde (C4H8O) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D

13. 1-Hexyne (C6H10) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D E

14. Butylamine (C4H11N) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D E

15. Benzoic acid (C7H6O2) 89.56 MHz (CDCl3)
Assign. Shift (ppm) A B C D

16. 13C NMR

17. Hexane (C6H14 ) 25.16 MHz (CDCl3) ppm Int. Assign. 31.87 1000 1

18. Octane (C8H18 ) 25.16 MHz (CDCl3) ppm Int. Assign. 32.15 1000 1

19. Cyclohexane (C6H12 ) 25.16 MHz (CDCl3)
ppm Int. Assign.

20. Toluene (C7H8) 25.16 MHz (CDCl3)
ppm Int. Assign.

21. p-Xylene (C8H10) 25.16 MHz (CDCl3)
ppm Int. Assign.

22. o-Xylene (C8H10) 25.16 MHz (CDCl3)
ppm Int. Assign.

23. m-Xylene (C8H10) 25.16 MHz (CDCl3)
ppm Int. Assign.

24. Ethyl acetate (C4H8O2) 15.09 MHz (CDCl3)
ppm Int. Assign.

25. Cyclopentanone (C5H8O) 25.16 MHz (CDCl3)
ppm Int. Assign.

26. Benzoic acid (C7H6O2) 25.16 MHz (CDCl3)
ppm Int. Assign.

27. p-Bromoaniline (C6H6BrN ) 25.16 MHz (CDCl3)
ppm Int Assign.

28. Diethyl ether (C4H10O) 25.16 MHz (CDCl3)
ppm Int. Assign.