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  2. C5H10O2 - Wikipedia

    en.wikipedia.org/wiki/C5H10O2

    The molecular formula C 5 H 10 O 2 (molar mass: 102.13 g/mol) may refer to: tert-Butyl formate; Ethyl propionate; Hydroxypivaldehyde; Isobutyl formate; Isopropyl acetate; Methylbutanoic acids. 2-Methylbutanoic acid; 3-Methylbutanoic acid (isovaleric acid) Methyl butyrate; Methyl isobutyrate; Pivalic acid; Propyl acetate; Tetrahydrofurfuryl ...

  3. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    [2] [3] The term metamer was formerly used for the same concept. [4] For example, butanol H 3 C−(CH 2) 3 −OH, methyl propyl ether H 3 C−(CH 2) 2 −O−CH 3, and diethyl ether (H 3 CCH 2 −) 2 O have the same molecular formula C 4 H 10 O but are three distinct structural isomers. The concept applies also to polyatomic ions with the same ...

  4. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    Isomers with the molecular formula C 5 H 10 with CAS numbers C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes .

  5. Isobutyl formate - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_formate

    Isobutyl formate (2-methylpropyl methanoate) is an organic ester with the chemical formula C 5 H 10 O 2. It is formed by the Fischer esterification of isobutanol with formic acid, with the aid of an acid catalyst. It is used as a flavor and fragrance ingredient because of its odor which is sweet, ethereal, and slightly fruity. [2] [3]

  6. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    In the case of water, with its 104.5° HOH angle, the OH bonding orbitals are constructed from O(~sp 4.0) orbitals (~20% s, ~80% p), while the lone pairs consist of O(~sp 2.3) orbitals (~30% s, ~70% p). As discussed in the justification above, the lone pairs behave as very electropositive substituents and have excess s character.

  7. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    In chemistry an eclipsed conformation is a conformation in which two substituents X and Y on adjacent atoms A, B are in closest proximity, implying that the torsion angle X–A–B–Y is 0°. [1] Such a conformation can exist in any open chain, single chemical bond connecting two sp 3-hybridised atoms, and it is normally a conformational ...

  8. Woodward's rules - Wikipedia

    en.wikipedia.org/wiki/Woodward's_rules

    With the aid of these rules the UV absorption maximum can be predicted, for example in these two compounds: [8] In the compound on the left, the base value is 214 nm (a heteroannular diene). This diene group has 4 alkyl substituents (labeled 1,2,3,4) and the double bond in one ring is exocyclic to the other (adding 5 nm for an exocyclic double ...

  9. C5H10O - Wikipedia

    en.wikipedia.org/wiki/C5H10O

    The molecular formula C 5 H 10 O may refer to: Isoprenol; Isovaleraldehyde (3-methylbutanal) 2-Methylbutanal; Methyl isopropyl ketone; 2-Methyltetrahydrofuran; 3-Methyltetrahydrofuran; Pentanal; 2-Pentanone; 3-Pentanone; Pivaldehyde (2,2-dimethylpropanal) Prenol; Tetrahydropyran