On Curvilinear Regression Analysis via Newly Proposed Entropies for Some Benzene Models

Table 1

The physical characteristics of benzene derivatives.

Chemical structures
Benzene	47.69	0.66	121.68	323.79	2.03	263.5	25.28
Naphthalene	38.97	1.67	252.38	484.95	3.03	409.5	42.45
Phenanthrene	32.43	2.68	383.08	586.11	4.03	555.5	59.62
Anthracene	32.43	2.68	383.08	586.11	4.03	555.5	59.62
Chrysene	27.41	3.69	513.78	650.8	5.03	701.5	76.79
Benz[a]anthrene	27.41	3.69	513.78	650.8	5.03	701.5	76.79
Triphenylene	27.41	3.69	513.78	650.8	5.03	701.5	76.79
Tetracene	27.41	3.69	513.78	650.8	5.9	701.5	76.79
Benzo[a]pyrene	26.08	4.48	621.88	689.17	5.34	765.5	85.53
Benzo[e]pyrene	26.08	4.48	621.88	689.17	5.34	765.5	85.53
Perylene	26.08	4.48	621.88	689.17	5.34	765.5	85.53
Benzo[ghi]perylene	24.85	5.27	729.98	728.06	5.66	829.5	94.28
Dibenzo[a, c]anthracene	23.47	4.7	644.48	714.53	6.02	847.5	93.96
Dibenzo[a, h]anthracene	23.47	4.7	644.48	714.53	6.02	847.5	93.96
Dibenzo[a, j]anthracene	23.47	4.7	644.48	714.53	6.02	847.5	93.96
Picene	23.47	4.7	644.48	714.53	6.02	847.5	93.96
Coronene	23.7	6.06	838.08	767.68	5.98	893.5	103.02
Pyrene	30.73	3.47	491.18	625.65	5.08	619.5	68.36