- Messages
- 381
- Reaction score
- 140
- Points
- 53
I'm sorry, but I still don't understand q.6, q.29 why is c not acidic(there is co2h bonded to it).6. Use pV=nRT.
8. Volume is proportional to temperature at constant pressure. You can tell from pV=nRT.
27. Unreactive towards mild oxidising agents = tertiary alcohol. We can get only D from a tertiary alcohol.
29. B and C are not acidic; A is not chiral. That leaves D.
30. The acid used to make this ester is hexanoic acid. Only C shows a hexanoate.
38. Step 1 will give us the product so we won't need steps 2 and 3.
21. Any C=C bond breaks and is replaced with a C=O bond.
29. Draw propanone first, then break the double bond and add an H to the O and a -CN bond. The remove the CN and put CO2H in its place.
30. (30+30)-18(water).
39. Compounds 1 and 2 are formed by the reaction of C3H7 radicals. Compound 3 is formed by the reaction of a C4H9 radical with a C2H5 radical. These last can't be made if only propanone is used.