How are methyl groups electron donating to the phenyl ring? Give a detailed explanation.
Reasons for electron donating nature of methyl group:
1)
Commonly written as Ar-CH3 (Ar-any phenyl ring) is electron
donating because of high magnitude of electron
cloud being collected over carbon.
Since carbon is less electronegitive, it do not possess the
required nuclear attraction to hold electrons.
2)
They activate the aromatic ring by increasing the
electrondensity on the ring through an
inductive donatingeffect.
This is the same effect that allows alkyl groups to stabilise
simple carbocations.
3)
The electrons in the three C-H bonds of the methyl are drown
towards the carbon atom, which causes the fourth valence electron
(in the 2px orbital) of the carbon atom to be pushed further away
from the nucleus (thus it is at a higher energy level) due to extra
repulsion from the C-H electrons.
If this fourth electron is part of a covalent bond (shared pair of electrons) with another atom, y, then the electrons in the C-y bond will be pushed further towards the y atom (again due to the extra repulsion from the three pairs of bonding electrons) making it more delta negative.
Hence, the CH3 group is said to be electron donating.
How are methyl groups electron donating to the phenyl ring? Give a detailed explanation.
what's the principles and of Electron-withdrawing groups and Electron-donating groups , why they give or accept electrons , especially in aromatic ring that act both donating and withdrawing? and please numerate members of each groups briefly?
What roles do electron withdrawing groups and electron donating groups play? (i.e., do they activate the diene or dienophile?
Which of the following are electron donating groups? -CH -NO, -COCH O-OCH - NHCOCH -CN Question 2 2 Which of the functional groups can act as a hydrogen bond donor? Select all that apply Carboxylic acid Alcohol D Amine Ester Aromatic ring Ether Amide Ketone
5. All electron-donating groups are activating groups and all are ortho-para directors with the exception of substituents, all electron-withdrawing groups are deactivating groups and all are meta directors. A. hydroxyl B. amino C. halogens D. alkoxyl 6. Hydrogen abstraction from the methyl group of methylbenzene (toluene) produces a radical called the radical. A. allylic B. free C. halogen D. benzyllic 7. The stability of benzyllic radicals can be explained by theory. A. resonance B. bond order C. inductive D. molecular...
Identify the substituent groups on the alkenes below as electron
withdrawing or electron donating by putting EWG or EDG after the
structure letter.
CN A B с D E
(1) indicate if the ring substituent is Electron Donating (EDG), Electron Withdrawing (EWG) or Neither (N): (11) rank them in order of their reactivity towards EAS (1 = fast........4 = slow) en T-Br -NO, NO2 TOCH; -OCH;
3. (2 points) Which of the following compounds have electron withdrawing (EWG) or electron donating groups (EDG)? Circle the positions that will be activated/deactivated?
3. (2 points) Which of the following compounds have electron withdrawing (EWG) or electron donating groups (EDG)? Circle the positions that will be activated/deactivated? NH2 NO₂
Please give a detailed explanation with a sketch if
necessary.
Imagine an electron trapped in a potential well along the x axis. The well is of finite depth. You can not raise or lower the potential, but you can shrink or expand the x-dimension of the well. What is your best strategy to hold the electron as long as possible?
please post detailed explanation
Problem 4: My wedding ring is rolling down an incline of 0 - 15º that has a friction coefficient of x=0.1. The ring has a mass of 5-g and a diameter of 2.5 cm. If the ring was initially at rest, what is its angular acceleration and how much time does it take to roll 0.2 meters? 0