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Tautomer energy comparison

using model chemistry: MP2/6-31G**

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 -20 -7 allene propyne -13
C4H6 sketch of 1,2-Butadiene sketch of 1,3-Butadiene -50 -51 1,2-Butadiene 1,3-Butadiene 1
C4H6 sketch of 1,2-Butadiene sketch of 1-Butyne -10 3 1,2-Butadiene 1-Butyne -13
C4H6 sketch of 1,2-Butadiene sketch of 2-Butyne -32 -17 1,2-Butadiene 2-Butyne -15
C4H6 sketch of Cyclobutene sketch of 1,3-Butadiene -38 -49 Cyclobutene 1,3-Butadiene 11
C4H6 sketch of 1-Methylcyclopropene sketch of 1,2-Butadiene -59 -82 1-Methylcyclopropene 1,2-Butadiene 23
C4H6 sketch of Methylenecyclopropane sketch of 1-Methylcyclopropene 38 42 Methylenecyclopropane 1-Methylcyclopropene -4
C3H6O sketch of Oxetane sketch of Propanal -118 -110 Oxetane Propanal -8
C4H8 sketch of cyclobutane sketch of 1-Butene -16 -33 cyclobutane 1-Butene 17
C3H4O2 sketch of 2-Propenoic acid sketch of β–Propiolactone 29 29 2-Propenoic acid β–Propiolactone 0
C4H6S sketch of Thiophene, 2,5-dihydro- sketch of Thiophene, 2,3-dihydro- -2 4 Thiophene, 2,5-dihydro- Thiophene, 2,3-dihydro- -7
C5H8 sketch of 1,3-Pentadiene, (E)- sketch of 1,4-Pentadiene 31 25 1,3-Pentadiene, (E)- 1,4-Pentadiene 5
C5H8 sketch of 1,3-Pentadiene, (E)- sketch of 1,2-Pentadiene 63 64 1,3-Pentadiene, (E)- 1,2-Pentadiene -1
C5H8 sketch of 1,2-Butadiene, 3-methyl- sketch of 1,3-Butadiene, 2-methyl- -48 -52 1,2-Butadiene, 3-methyl- 1,3-Butadiene, 2-methyl- 3
C5H10 sketch of 1-Butene, 2-methyl- sketch of 2-Butene, 2-methyl- -8 -5 1-Butene, 2-methyl- 2-Butene, 2-methyl- -3
C5H10 sketch of Cyclopropane, 1,1-dimethyl- sketch of 1-Butene, 2-methyl- -13 -29 Cyclopropane, 1,1-dimethyl- 1-Butene, 2-methyl- 16