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  2. C12H22O11 - Wikipedia

    en.wikipedia.org/wiki/C12H22O11

    The molecular form C 12 H 22 O 11 (molar mass: 342.29 g/mol, exact mass : 342.116212) may refer to: Disaccharides. Allolactose; Cellobiose; Galactose-alpha-1,3-galactose;

  3. Sucrose - Wikipedia

    en.wikipedia.org/wiki/Sucrose

    H 2 SO 4 (catalyst) + C 12 H 22 O 11 → 12 C + 11 H 2 O + heat (and some H 2 O + SO 3 as a result of the heat). The formula for sucrose's decomposition can be represented as a two-step reaction: the first simplified reaction is dehydration of sucrose to pure carbon and water, and then carbon is oxidised to CO 2 by O 2 from air. C 12 H 22 O 11 ...

  4. C12H22O - Wikipedia

    en.wikipedia.org/wiki/C12H22O

    The molecular formula C 12 H 22 O (molar mass: 182.307 g/mol, exact mass: 182.1671 u) may refer to: Cyclododecanone; Geosmin

  5. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    As such, cyclobutane is unstable above about 500 °C. The four carbon atoms in cyclobutane are not coplanar; instead, the ring typically adopts a folded or "puckered" conformation. [2] This implies that the C-C-C angle is less than 90°. One of the carbon atoms makes a 25° angle with the plane formed by the other three carbons.

  6. Cyclopropane - Wikipedia

    en.wikipedia.org/wiki/Cyclopropane

    The triangular structure of cyclopropane requires the bond angles between carbon-carbon covalent bonds to be 60°. The molecule has D 3h molecular symmetry. The C-C distances are 151 pm versus 153-155 pm. [15] [16] Despite their shortness, the C-C bonds in cyclopropane are weakened by 34 kcal/mol vs ordinary C-C bonds.

  7. Disiloxane - Wikipedia

    en.wikipedia.org/wiki/Disiloxane

    In contrast, the C−O−C bond angle in the carbon analogue of disiloxane, dimethyl ether, is 111°. [ 4 ] The unusual bond angle in disiloxane has been attributed primarily to negative hyperconjugation between oxygen p orbitals and silicon–carbon σ* antibonding orbitals, p (O) → σ*(Si􏰉−R), a form of π backbonding .

  8. Ketene - Wikipedia

    en.wikipedia.org/wiki/Ketene

    Ethenone, the simplest ketene, has different experimental lengths for each of the double bonds; the C=O bond is 1.160Å and the C=C bond is 1.314Å. The angle between the two H atoms is 121.5°, similar to the theoretically ideal angle formed in alkenes between sp 2 carbon atom and H substituents. [5] Ketenes are unstable and cannot be stored.

  9. Pentane - Wikipedia

    en.wikipedia.org/wiki/Pentane

    Pentane is an organic compound with the formula C 5 H 12 —that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane ...