Removing the tip of the stem in a young plant will most directly interfere with the production of
1 answer:
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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.
Data:
m (<span>Sample Mass) = ?
n (</span><span>Number of moles) = 0.714 mol
MM (Molar Mass) of </span>Mercury (I) Chloride (
)
Hg = 2*200.59 = 401.18 amu
Cl = 2*35.453 = 70.906 amu
----------------------------------------
Molar Mass
= 401.18 + 70.906 = 472.086 ≈ 472.09<span> amu or 472.09 g/mol
</span>
Formula:
Solving:
Answer:
By approximation would be letter D) <span>337.2 g</span>
m (<span>Sample Mass) = ?
n (</span><span>Number of moles) = 0.714 mol
MM (Molar Mass) of </span>Mercury (I) Chloride (
Hg = 2*200.59 = 401.18 amu
Cl = 2*35.453 = 70.906 amu
----------------------------------------
Molar Mass
</span>
Formula:
Solving:
Answer:
By approximation would be letter D) <span>337.2 g</span>