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List of experimental bond angles of type aCCO

Bond angles in degrees.
Click on an entry for more experimental geometry data.
Bond type Species Name Angle Comment
aCCO C2H4O Ethylene oxide 59.20 from symmetry
aCCO C3H6O Oxetane 91.80
aCCO C3H6O2 1,3-Dioxolane 101.00
aCCO C4H8O2 1,3-Dioxolane, 2-methyl- 105.20
aCCO CH3CH(CH3)ONO Isopropyl nitrite 107.60 assumed
aCCO C4H10O Propane, 2-methoxy- 107.70
aCCO CH3CH2OH Ethanol 107.80
aCCO C2H6O2 1,2-Ethanediol 107.80 !assumed
aCCO C3H8O2 1,3-Propanediol 108.00 to O with H that hydrogen bonds to other O
aC=CO C3H3NO Oxazole 108.10
aCCO C3H8O2 Propylene glycol 108.10
aCCO CH3OC2H5 Ethane, methoxy- 108.15
aCCO C4H8O2 Ethyl acetate 108.20
aCCO C4H2O3 Maleic Anhydride 108.20
aCCO C4H10O Ethoxy ethane 108.40
aC=CO C3H2O3 vinylene carbonate 108.67
aCCO C4H10O Methyl propyl ether 108.80
aCCO C4H8O2 1,3-Dioxane 109.20
aCCO C2H5NO3 Nitric acid, ethyl ester 109.47 !assumed
aCCO CH3CH(NH2)COOH Alanine 110.30
aCCO CH3COOH Acetic acid 110.60
aC=CO C3H3NO Isoxazole 110.60
aC=CO C4H4O Furan 110.70
aC=CO C4H5NO Isoxazole, 5-methyl- 110.70 !assumed
aC=CO C4H5NO 3-Methylisoxazole 110.70 !assumed
aCCO C4H8O2 1,3-Dioxolane, 2-methyl- 110.90 to methyl
aCCO CF3COOH trifluoroacetic acid 111.10
aCCO HOCH2COOH Hydroxyacetic acid 111.30
aCCO H2NCH2COOH Glycine 111.50
aCCO C3H6O 2-Propen-1-ol 111.80
aCCO C4H8O2 Ethyl acetate 111.90 dependent
aCCO C5H10O 2H-Pyran, tetrahydro- 112.00
aCCO C3H8O2 1,3-Propanediol 112.00 to O receiving the H bond
aCCO HOCH2COOH Hydroxyacetic acid 112.60
aCCO C4H10O2 Ethane, 1,2-dimethoxy- 113.20
aCCO C4H10O Propane, 2-methoxy- 113.70
aCCO C3H5ClO Oxirane, (chloromethyl)- 114.00
aCCO CH3CH2O Ethoxy radical 114.40
aCCO C4H5NO Isoxazole, 5-methyl- 116.00 !assumed
aC=CO CH2CHOCHCH2 Vinyl ether 119.00
aCC=O C4H6O2 2,3-Butanedione 120.30
aCC=O C5H10O 2-Butanone, 3-methyl- 120.80
aCC=O C2H2O2 Ethanedial 121.20
aCC=O C5H8O Methyl cyclopropyl ketone 121.80 !average
aCC=O CH3COCH3 Acetone 122.00
aCC=O CH3CONH2 Acetamide 122.90 derived from aCCN and aNC=O
aCC=O CH3COCH2CH3 2-Butanone 122.90 central carbons
aCC=O C2H2O4 Oxalic Acid 123.10
aCC=O CHOCHCHCH3 2-Butenal 123.28 !assumed
aCC=O CHOCH(CH3)CH3 Propanal, 2-methyl- 123.30
aCC=O CH2ClCHO chloroacetaldehyde 123.30
aC=CO C5H8O 2H-Pyran, 3,4-dihydro- 123.40 !assumed
aCC=O CH2CHCHO Acrolein 123.90
aCC=O CH3CHO Acetaldehyde 123.90
aCC=O C4H8O2 Ethyl acetate 124.10
aCC=O HCCCHO 2-propynal 124.20
aCC=O HOCH2COOH Hydroxyacetic acid 124.20
aCC=O ClCOClCO Oxalyl chloride 124.20
aCC=O CH2CHCHO Acrolein 124.30
aCC=O CH3CH2CHO Propanal 124.40
aCC=O C6H12O hexanal 124.58
aCC=O C5H4O2 4-Cyclopentene-1,3-dione 124.90
aCC=O H2NCH2COOH Glycine 125.00
aCC=O CH3CH(NH2)COOH Alanine 125.60
aC=CO CH2C(CH3)OCH3 1-Propene, 2-methoxy- 125.80
aCCO CH2CHOH ethenol 126.20
aCC=O CH3COOH Acetic acid 126.60
aCC=O CF3COOH trifluoroacetic acid 126.80
aCC=O CH3COF Acetyl fluoride 128.35
aCC=O C4H2O3 Maleic Anhydride 129.20
aCC=O C3H4O Cyclopropanone 147.70 by symmetry
aC=C=O C3O2 Carbon suboxide 179.20 crystal structure
aC=C=O C3H4O Methylketene 180.00
Average 117.42 ±15.13
Min 59.20
Max 180.00