Answer:
Explanation:
In the following reaction we have shown an example of aromatic substitution reaction .
C₆H₆ + RCl = C₆H₅R + HCl
This reaction takes place in the presence of catalyst like AlCl₃ which is a lewis acid .
First of all formation of carbocation is made as follows .
RCl + AlCl₃ = R⁺ + AlCl₄⁻
This R⁺ is carbocation which is also called electrophile . It attacks the ring to get attached with it .
C₆H₆ + R⁺ = C₆H₅R⁺H.
The complex formed is unstable , though it is stabilized by resonance effect . In the last step H⁺ is kicked out of the ring . The driving force that does it is the steric hindrance due to presence of two adjacent group of H and R⁺ at the same place . Second driving force is attack by the base AlCl₄⁻ that had been formed earlier . It acts as base and it extracts proton ( H⁺ ) from the ring .
C₆H₅R⁺H + AlCl₄⁻ = C₆H₆ + AlCl₃ + HCl .
The formation of a stable product C₆H₆ also drives the reaction to form this product .
Answer: The p orbital can hold up to six electrons. We'll put six in the 2p orbital and then put the remaining electron in the 3s. Therefore the sodium electron configuration will be 1s22s22p63s1.
Explanation:
The sand to pass through, but not the gravel. Hope this helps!
Answer:51.1%
Explanation:
Mass percent : It is defined as the mass of the given component present in the total mass of the compound. Formula used : First we have to calculate the mass of and . Mass of = 18 g/mole Mass of = 7 × 18 g/mole = 126 g/mole Mass of = 246.47 g/mole Now put all the given values in the above formula, we get the mass percent of in . Therefore, the mass percent of in is, 51.1%
