Answer:
Explanation:
The movement of the electrons is illustrated in the picture attached to this answer. It is a four-step reaction mechanism.
First STEP: The first step involves the transfer of an electron from sodium to form a radical anion.
Second STEP: This radical anion then removes a proton/hydrogen from ammonia in a bid to neutralize itself (hence the hydrogen becomes bonded to the anion).
Third STEP: The sodium (from NaNH₂ formed) transfers an electron again to produce a vinyl carbanion.
Fourth STEP: The carbanion then removes a proton/hydrogen from ammonia (like in the second step) to form a neutral trans-alkene.
NOTE: The circled numbers denote each step while the mechanism on the left represents the use of any alkyl group (R and R') while the mechanism on the right assumes both alkyl groups are methyl. Hence, 2-butyne started the reaction and the final product was trans-2-butene.
Answer: Uhm you answered your own question...
Explanation:
Answer:
Empirical formula of C₈H₈ = CH
Explanation:
Data Given:
Molecular Formula = C₈H₈
Empirical Formula = ?
Solution
Empirical Formula:
Empirical formula is the simplest ration of atoms in the molecule but not all numbers of atoms in a compound.
So,
tha ration of the molecular formula should be divided by whole number to get the simplest ratio of molecule
C₈H₈ Consist of Carbon (C), and Hydrogen (H)
Now
Look at the ratio of these two atoms in the compound
C : H
8 : 8
Divide the ratio by two to get simplest ratio
C : H
8/8 : 8/8
1 : 1
So for the empirical formula is the simplest ratio of carbon to hydrogen 1 : 1
So the empirical formula will be
Empirical formula of C₈H₈ = CH
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