Answer: Benzene is less reactive than methylbenzoate and more reactive than Nitrobenzene
Explanation:
This is because the methyl group on the benzene ring is an electron donating group leading to the activation of the ring and subsequently leading to more canonical resonance structure at the intermediate stage of the reaction enhancing the faster reactivity
However for the Nitrobenzene the nitro group is an electron withdrawing group leading to a slower activation and less resonance canonical structure at the reaction intermediate leading to a slower reaction than the reaction of benzene without the nitro group
Answer:
1-bromo-1-tert-butylcyclohexane
Explanation:
The parent compound comprises of a cyclohexane to with a tertiary butyl carbon attached. We have been told that the reaction occurs by radical mechanism hence we must recall the order of stability of radicals: tertiary>a secondary> a primary. This implies that the reaction will occur at carbon 1 of the cyclohexane which is a tertiary carbon atom. This leads to the formation of a radical at the 1-position and bromination at that position hence the answer chosen above.
Explanation:
1)
The Kc for the reverse reaction is the inverse of the Kc of the reaction:
2)
The Kc for the reverse reaction is the inverse of the Kc of the reaction:
3)
The Kc for the reverse reaction is the inverse of the Kc of the reaction:
Answer:
- Mixtures can be separated using a variety of techniques.
- Chromatography involves solvent separation on a solid medium.
- Distillation takes advantage of differences in boiling points.
- Evaporation removes a liquid from a solution to leave a solid material.
- Filtration separates solids of different sizes.
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Answer:
Displacement is the direction from the starting point and the length of a directly line from the starting point to the ending point.