WebSolution Verified by Toppr Correct option is C) Stability of carbanions decreases in order: 1 o>2 o>3 o. IV is most stable due to resonance between negative charge and double bond of benzene ring. I is more stable than II and III as CH 3CH 2CH 2CH 2− is 1 o .II is more stable than III as CH 3CH −CH 2CH 3 is 2 o. WebHence, O2NCH2CH2O-is expected to be more stable than CH3CH2O-. Q10 : Explain why alkyl groups act as electron donors when attached to a À system. Answer : When an alkyl group is attached to a À system, it acts as an electron-donor group by the process of hyperconjugation.
O2NCH2CH2O^- and CH3CH2O^- which of the two is expected …
WebAnswer (1 of 4): First we should have clearity about what is covalent character in ionic bond. All ionic bonds are not purely ionic as nothing in universe is 100% pure. So it has some directional nature, which we called as polarizibility in chemistry. Higher the directional nature , … Web21 de dic. de 2024 · Expert Answer CH3CH2CH2CH2+ is more stable than (CH2)2CHCH2+ because it is having more alpha hydrogen. Due to presence of more alpha hydrogen, It will show more hyperconjugaion effect. Answered by Ravi 21 Dec, 2024, 10:47: AM Practice Test Webinar All Questions Ask a Doubt Answered Unanswered My … park city lifts summer
Which is more stable O2NCH2CH2O or CH3CH2O and why? - Byju
WebCH3O- is a strong base. correctly reflects the relationship between base strength and nucleophilicity Across a period (left to right) nucleophilicity decreases as base strength decreases For two nucleophiles with the same nucleophilic atom, the stronger base is the stronger nucleophile. http://sistemasp.tehuacan.gob.mx/tvfuasxa/are-alkenes-more-reactive-than-alkynes Web14 de dic. de 2024 · o2NCH2CH2O- is more stable than CHCH2O- because NO2 shows -R and -I effect which reduces the electron density at O- so it stablises but CH3 hav +I … park city light parade