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Electron withdrawing groups decrease the reactivity of a molecule by pulling electron density away from the reacting center, making it less likely to participate in reactions. Electron donating groups increase reactivity by pushing electron density towards the reacting center, making it more likely to participate in reactions.

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4mo ago

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Is the molecule an electron donating or withdrawing group?

The molecule is an electron donating group.


How do electron donating groups differ from electron withdrawing groups in terms of their impact on the reactivity of molecules?

Electron donating groups increase the electron density of a molecule, making it more reactive, while electron withdrawing groups decrease the electron density, making the molecule less reactive.


Is the methyl group in a molecule electron donating or withdrawing?

The methyl group in a molecule is electron donating.


What is the difference between electron donating groups and electron withdrawing groups in terms of their impact on the reactivity of organic molecules?

Electron donating groups increase the electron density of a molecule, making it more reactive, while electron withdrawing groups decrease the electron density, making the molecule less reactive.


How do electron withdrawing groups, such as ketones, affect the reactivity of organic compounds?

Electron withdrawing groups, like ketones, decrease the reactivity of organic compounds by pulling electron density away from the molecule, making it less likely to participate in chemical reactions.


What is the Hammet substituent constant?

The Hammet substituent constant shows the electron donating or accepting nature of the molecule as well as its chemical reactivity. It is often used in the QSAR study of drugs.


How does the presence of a phenyl group affect the electron-withdrawing properties of a molecule?

The presence of a phenyl group in a molecule increases its electron-withdrawing properties. This is because the phenyl group contains a delocalized pi-electron system, which can withdraw electrons from the rest of the molecule, making it more electron-deficient.


Is alkyle group is electron withdrawing?

Alkyl groups are generally electron donating due to their inductive effect, where they push electron density towards the rest of the molecule. This is because alkyl groups are less electronegative than carbon and hydrogen, leading to a slight positive charge that can stabilize adjacent negative charges.


Why does electron withdrawing groups increase acidity?

Assuming the groups are conjugated to the acid/base groups: An acid wants to lose a proton. When it loses a proton, you form an anion (or a neutral molecule, but when talking about electron donating/withdrawing groups, you assume there is a charge). The more stable the anion, the more easily the proton comes off, and the more acidic it is. A base is the opposite. A base gains a proton to become cationic. The more stable the cation, the more likely it is to pick up a proton, and the more basic it is. An electron withdrawing group can stabilize an anion (and thus make something more acidic) and an electron donating group can stabilze a cation (and make something more basic). The opposites also hold true: an electron donating group can destabilize an anion and make something less acidic, and vice versa for bases.


List of electron withdrawing group?

Some common electron-withdrawing groups include nitro (-NO2), carbonyl (e.g. -CO), cyano (-CN), and halogens (e.g. -F, -Cl, -Br, -I). These groups are able to pull electron density away from the rest of the molecule through inductive or resonance effects, making the molecule more electrophilic.


Explain dipole movement of a molecule with respect to Inductive effect?

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What is the CO2 electron count and how does it impact the molecule's reactivity?

Carbon dioxide (CO2) has a total of 16 electrons. The molecule's reactivity is impacted by its electron count, as CO2 is a stable molecule due to its linear structure and the sharing of electrons between carbon and oxygen atoms. This stability makes it less reactive compared to other molecules with more available electrons for bonding.