Structure I below underwent ligand exchange with CO to give only mer-2, which later rearranged to fac-2. Treatment of 1 with P(CD,), gave 3, showing that ligand exchange occurred only trans to the SiMe, group. An X-ray analysis of 1 indicated that other than the length of the Ru-P bond located trans to H, the next longest Ru-P bond was situated trans to the SiMe, group.122 L. L SiMez Ru H. L SiMea CRu H, SiMez Ru H. + CO L' OC- L = PMe3 1 mer-2 Jaс-2 P(CD3)3 SiMez CRu. H. (CDy) P" 3. a. How do the trans effect and trans influence of the SiMe, group com- pare with those of phosphines? Explain? b. What is the driving force for the rearrangement of mer-2 to fac-2?
Carbohydrates
Carbohydrates are the organic compounds that are obtained in foods and living matters in the shape of sugars, cellulose, and starch. The general formula of carbohydrates is Cn(H2O)2. The ratio of H and O present in carbohydrates is identical to water.
Starch
Starch is a polysaccharide carbohydrate that belongs to the category of polysaccharide carbohydrates.
Mutarotation
The rotation of a particular structure of the chiral compound because of the epimerization is called mutarotation. It is the repercussion of the ring chain tautomerism. In terms of glucose, this can be defined as the modification in the equilibrium of the α- and β- glucose anomers upon its dissolution in the solvent water. This process is usually seen in the chemistry of carbohydrates.
L Sugar
A chemical compound that is represented with a molecular formula C6H12O6 is called L-(-) sugar. At the carbon’s 5th position, the hydroxyl group is placed to the compound’s left and therefore the sugar is represented as L(-)-sugar. It is capable of rotating the polarized light’s plane in the direction anticlockwise. L isomers are one of the 2 isomers formed by the configurational stereochemistry of the carbohydrates.
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