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My answer to the question is 0.00000051
Answer:
The Fischer Projection formula of D-glucose is as shown in the attachment below.
The chiral centre that determines its name is the last carbon from the carbonyl group, C-6
Explanation:
Fisher projection formulas are used to show sugars in their open chain form. In a Fischer projection, the carbon atoms of a sugar molecule are joined vertically by solid lines, while carbon-oxygen and carbon-hydrogen bonds are joined horizontally using solid lines as well.
The horizontal bonds project out of the plane of the paper or screen towards the reader whereas vertical bonds project behind the plane of the paper or screen, away from the reader.
Glucose is an aldose sugar with two different optical isomers or enantiomers, D-glucose and L-glucose. The designation D- or L- depends on the configuration of the chiral or asymmetric carbon most distant from the carbonyl carbon of glucose. If the chiral carbon has the same configuration as D-glyceraldehyde, that the -OH roup on the right side of the carbon and -H group on the left, it is snamed D-glucose. However, if the chiral carbon has the same configuration as L-glyceraldyde, that is with the -OH group on the right and the -H group on the right, it is named L-glucose
Homogeneous Reactions. At equilibrium, the rate of the forward and reverse reaction are equal, which is demonstrated by the arrows. The equilibrium constant, however, gives the ratio of the units (pressure or concentration) of the products to the reactants when the reaction is at equilibrium.
Answer:
a double replacement reaction, because the hydrogen of the acid change places with the potassium of the base, forming salt and water...
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From these two experiments, Thomson concluded, "I can see no escape from the conclusion that (cathode rays) are charges of negative electricity carried by particles of matter."
Explanation:
I have done a poster board on him about this :) i hope this helps