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ioda
3 years ago
8

Explain why c6h5ch2ch2br is not formed during the radical bromination of c6h5ch2ch3. select the single best answer.

Chemistry
1 answer:
gtnhenbr [62]3 years ago
7 0
Hi!

The radical bromination reaction of C₆H₅CH₂CH₃ is performed through a mechanism in which radical reactions are involved. This compound is an alkylbenzene compound, and the carbon that is more reactive towards radical bromination is the carbon bonded to the aromatic ring because in the reaction mechanism the intermediaries are stabilized by resonance in the aromatic ring. 

A terminal substitution will not occur because substitution there will not be stabilized by resonance. The compound that will be formed in this reaction would be:

C₆H₅CH₂CH₃ + Br₂ → C₆H₅CH₂(Br)CH₃ + HBr
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Crank

Answer:

Option D. Al is above H on the activity series.

Explanation:

The equation for the reaction is given below:

2Al + 6HBr —> 2AlBr₃ + 3H₂

The activity series gives us a background understanding of the reactivity of elements i.e how elements displace other elements when present in solution.

From the activity series of metals, we understood that metal higher in the series will displace those lower in the series.

Considering the equation given above, Al is higher than H in the activity series. Thus, the reaction will proceed as illustrated by the equation.

Therefore, we can conclude that the reaction will only occur if Al is higher than H in the activity series.

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Answer:

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Explanation:

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CH_3COONa\ (aq) + HCl\ (aq)\longrightarrow CH_3COOH\ (aq) + NaCl\ (aq)\\\\

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CH_3COO^{-} \ (aq) + H^{+}\ (aq) \longrightarrow CH_3COOH \ (aq)

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