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Propane, structure

As shown in Table 1, a remarkable variety of alkene complexes bearing metal centers in a low oxidation state have been isolated and their structures have been determined by X-ray analysis. All the C-C bond distances in olefins coordinated to early transition metals at low oxidation states are more or less elongated compared to free ethylene. These structural data, together with those from NMR studies [14], indicate a major contribution of the metallacyclo-propane structure (2), a fact which is also supported by calculation studies [15]. In the case of ethylene bridging two metal centers such as [ Cp2ZrX 2(iu-f/-C2H4)] (3), the M-C bond could be characterized as a er-bond and there is a little contribution from the / -ethylene canonical structure [16-18]. [Pg.6]

This representation is called a structural formula, in which lines depict two electron bonds between atoms. Look at the propane structure and observe that the 4 bonds to each carbon complete its valence orbitals with 8 electrons. [Pg.58]

NAME 1.3 -Dibromo-2-(bromomethyl)-propane STRUCTURAL FORMULA... [Pg.227]

It is well established that steric effects hinder the Cope rearrangement of divinylcyclopropanes. An interesting example of this steric effect is seen in the reaction of 33 with cis- and trans-l-acetoxy-butadiene (Scheme 13). ° The reaction of 33 with trans-1-acetoxy-l, 3-butadiene leads cleanly to the [3+4] annulation product 34 in 67% yield. In contrast, the product from the reaction of 33 with c/j-l-ace-toxy- 1,3-butadiene is the cw-divinylcyclopropane 35 (80% yield), and high temperatures (220 °C) are required to convert 35 to the [3+4] annulation product 36. The effect of alkene geometry on the stereochemistry and the rate of reaction is readily explained by considering the boat transition state for the Cope rearrangement of divinylcyclo-propanes (structure 37). A trans diene substituent (Y) would generate a trans product (34), whereas a cis substituent (X) would lead to a cis... [Pg.134]

Phenolic wood extractives, flavones, and catechol derivatives. A large number of phenolic substances comprising wood extractives, lignin precursors, and other guaiacyl propane structures have been investigated by TLC on cellulose and on silica gel (110) which has also been used for the... [Pg.895]


See other pages where Propane, structure is mentioned: [Pg.146]    [Pg.100]    [Pg.46]    [Pg.271]    [Pg.20]    [Pg.14]    [Pg.440]    [Pg.146]    [Pg.321]    [Pg.389]    [Pg.324]    [Pg.320]    [Pg.210]    [Pg.32]    [Pg.44]    [Pg.452]    [Pg.353]    [Pg.46]   
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Propane 2.3- -, crystal structure

Propane electronic structure

Propane molecular structure

Propane structural formula

Structures of propane

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