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A valid lewis structure of __________ cannot be drawn without violating the octet rule. a valid lewis structure of __________ ca
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Answer:
The answer is E. All of the statements describe the anomeric carbon.
Explanation:
When a sugar switches from its open form to its ring form, the carbon from the carbonyl (aldehyde if it is an aldose, or a ketone in the case of a ketose) suffers a nucleophilic addition by one of the hydroxyls in the chain, preferably one that will form a 5 or 6 membered ring after the reaction.
As such, the anomeric carbon will have two oxygens attached (The original one and the one that bonded when the ring closed).
It will be chiral, given that it has 4 different groups attached. (-OR,-OH,-H and -R, where R is the carbon chain).
The hydroxyl group can be in any position (Above of below the ring), depending on with side the addition took place. (See attachment)
It is the carbon of the carbonyl in the open-chain form of the sugar, because it is the only one that can react with the Hydroxyls.
Answer:
Y = 92.5 %
Explanation:
Hello there!
In this case, since the reaction between lead (II) nitrate and potassium bromide is:
Exhibits a 1:2 mole ratio of the former to the later, we can calculate the moles of lead (II) bromide product to figure out the limiting reactant:
Thus, the limiting reactant is the KBr as it yields the fewest moles of PbBr2 product. Afterwards, we calculate the mass of product by using its molar mass:
And the resulting percent yield:
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