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Tautomer energy comparison

using model chemistry: TPSSh/6-31+G**

17 10 12 10 46
formula sketch Energy (kJ mol-1) Name difference
A B calculated experiment A B
C3H4 sketch of allene sketch of propyne 14 -7 allene propyne 21
C4H6 sketch of 1,2-Butadiene sketch of 1,3-Butadiene -44 -51 1,2-Butadiene 1,3-Butadiene 8
C4H6 sketch of 1,2-Butadiene sketch of 1-Butyne 25 3 1,2-Butadiene 1-Butyne 22
C4H6 sketch of Cyclobutene sketch of 1,3-Butadiene -44 -49 Cyclobutene 1,3-Butadiene 6
C4H6 sketch of 1-Methylcyclopropene sketch of 1,2-Butadiene -71 -82 1-Methylcyclopropene 1,2-Butadiene 11
C4H6 sketch of Methylenecyclopropane sketch of 1-Methylcyclopropene 48 42 Methylenecyclopropane 1-Methylcyclopropene 6
C3H6O sketch of Oxetane sketch of Propanal -98 -110 Oxetane Propanal 12
C4H8 sketch of cyclobutane sketch of 1-Butene -18 -33 cyclobutane 1-Butene 14
C3H4O2 sketch of 2-Propenoic acid sketch of β–Propiolactone 19 29 2-Propenoic acid β–Propiolactone -9
C4H6S sketch of Thiophene, 2,5-dihydro- sketch of Thiophene, 2,3-dihydro- -2 4 Thiophene, 2,5-dihydro- Thiophene, 2,3-dihydro- -6
C5H8 sketch of 1,3-Pentadiene, (E)- sketch of 1,4-Pentadiene 36 25 1,3-Pentadiene, (E)- 1,4-Pentadiene 10
C5H8 sketch of 1,3-Pentadiene, (E)- sketch of 1,2-Pentadiene 60 64 1,3-Pentadiene, (E)- 1,2-Pentadiene -4
C5H8 sketch of 1,2-Butadiene, 3-methyl- sketch of 1,3-Butadiene, 2-methyl- -43 -52 1,2-Butadiene, 3-methyl- 1,3-Butadiene, 2-methyl- 9
C5H10 sketch of Cyclopropane, 1,1-dimethyl- sketch of 1-Butene, 2-methyl- -17 -29 Cyclopropane, 1,1-dimethyl- 1-Butene, 2-methyl- 12
C5H10 sketch of 1-Butene, 2-methyl- sketch of 2-Butene, 2-methyl- -11 -5 1-Butene, 2-methyl- 2-Butene, 2-methyl- -5