Answer:
15.28 L
Explanation:
Use combined gas law and rearrange formula
Change C to K
- Hope that helped! Please let me know if you need further explanation, as I can show you step by step.
Answer:
A. Diethyl ether will react with the alkenes that were formed in the experiment.
Explanation:
Ethers such as diethyl ether dissolve a wide range of polar and nonpolar organic compounds. Nonpolar compounds are generally more soluble in diethyl ether than alcohols because ethers do not have a hydrogen bonding network that must be broken up to dissolve the solute.
Well, an independent variable ids the thing that stays the same and a dependent variable is the thing that changes.
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.
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BTW reduction is the action or fact of making a specified thing smaller or less in amount, degree, or size.