Arrange the following compounds in an increasing order of their property mentioned

1. ethanal, propanal, propanone, butanone.( reactivity in nucleophilic addition)

2. CH3 — CHO, CH3 — CH2 — OH, CH3 — CH2— CH3 (boiling points)
3. Benzoic acid, 4-Nitrobenzoic acid, 3,4-Dinitrobenzoic acid, 4-Methoxybenzoic acid
(acid strength)
4. CH3CH2CH (Br) COOH, CH3CH (Br) CH2COOH, (CH3)2CHCOOH, CH3CH2CH2COOH
(acid strength)
5. CH3CHO, CH3CH2OH, CH3OCH3, CH3COOH. ( boilingpoint)
6. C6H5NH2, NH3, C2H5NH2, (C2H5)2 NH ( pKb values)
7. (CH3)3N, (CH3)2NH, CH3NH2 ( basic strength )
8. (C2H5)2NH, (C2H5)3N, C2H5NH2 C2H5OH (boilingpoint)
9. (CH3)2NH, CH3NH2, C6H5NH2 (solubility in water)
10. (C2H5)3N, C2H5NH2, (C2H5)2NH ( base strength in gas phase)
11. C6H5CH2NH2, C6H5NHCH3, C6H5NH2 ( pKb values)
12. Aniline, p-nitroaniline and p-toluidine ( basic strength)
13. C2H5NH2, (C2H5)2NH, (C2H5)3N ( basic strength in gaseous state)
14. Phenol, ethanol, water (acidic nature)
15. Benzoic acid, Phenol, Cresol (acidic character)
16. CH3COCH3, HCHO, CH3CHO ,C6H5CHO (reactivity towards HCN)
17. Acetaldehyde, Acetone, Methyl tert-butyl ketone (reactivity towards HCN)
18. Benzoic acid, 3,4-Dinitrobenzoic acid, 4-Methoxybenzoic acid (acid strength)