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: Ions are formed by the addition of electrons to, or the removal of electrons from, neutral atoms or molecules or other ions; by combination of ions with other particles; or by rupture of a covalent bond between two atoms in such a way that both of the electrons of the bond are left in association with one of the ...
Answer: 1.32
Explanation:
First, we must obtain the molar mass of HBr. After that, we try to obtain the concentration of the hydrobromic acid from the formula n=CV since the volume of solution and mass of acid was provided. Recall that n=m/M. If the concentration of acid is thus obtained, we make use of the fact that the concentration of H+ in the acid is equal to the molar concentration of HBr to obtain the pH. The pH is the negative logarithm of the concentration we obtained in the initial step.
If you wanted to find a sample of fermium,which has an atomic mass of 100 I would look deep under the earth
