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Naddika [18.5K]
3 years ago
6

In the acid-catalyzed dehydration of 2−methyl−1−propanol, what carbocation would be formed if a hydride shift accompanied cleava

ge of the carbon-oxygen bond in the alkyloxonium ion?
Chemistry
1 answer:
Lorico [155]3 years ago
8 0

Answer:

t-butyl cation

Explanation:

Generally a dehydration reaction occurs when an organic compound loses  water molecules to form alkenes. However, in an acid-catalyzed dehydration, the dehydration reaction occurs in the presence of an acidic compound which acts as a catalyst. Therefore, for this specific case, the hydride will migrate and a t-butyl cation will be formed.  This is because it is more stable due to the presence of three electron releasing alkyl groups which can stabilize a positive charge compared with the secondary cation formed when the methyl group migrates.

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Answer:

4.5g/ml

Explanation:

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cylinder previously filled with water = 20.00 mL

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density = \frac{7.56}{(21.68 - 20.00)}

density = 4.5g/ml

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The Dilution of a buffer solution with a small amount of water will raise the PH of the solution. Dilution is the process of "reducing the concentration of a solute in a solution by simply adding more solvent to the solution, such as water." Dilution involves increasing the amount of solvent in a solution without increasing the amount of solute.

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2 years ago
Why does increasing the temperature of two reactants in solution make a
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5 0
3 years ago
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Explanation:

Hope this helps!

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3 years ago
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