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postnew [5]
3 years ago
12

Why are there so many different kind of apples

Chemistry
1 answer:
Mars2501 [29]3 years ago
8 0
There are many different types of apples i dont EXACTLY know why but however there are some eople that can only have a certain type of apple
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2 years ago
Which describes mendeleevs use of the term eka-aluminum??
solong [7]

a. A mixture of aluminum and an unknown element.

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What is a goal of the planned mission MIRI?
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2 years ago
Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. Use the wedge/hash bond
PolarNik [594]

Answer:

See the image 1

Explanation:

If you look carefully at the progress of the SN2 reaction, you will realize something very important about the outcome. The nucleophile, being an electron-rich species, must attack the electrophilic carbon from the back side relative to the location of the leaving group. Approach from the front side simply doesn't work: the leaving group - which is also an electron-rich group - blocks the way. (see image 2)

The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)

What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.

6 0
3 years ago
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