O2nch2ch2o- is more stable than ch3ch2o-
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. Webare alkenes more reactive than alkynes
O2nch2ch2o- is more stable than ch3ch2o-
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WebQuestion: CH3CH2O is more stable than CH3COO- CH3COO is resonance stabilized CH3CH2O is more basic than CH3COO- The stronger the acid, the weaker its conjugate base. This is known as the: Kekule statement The reverse relationship The inverse relationship The acid-base relationship The weak acid relationship Te pKa of a weak acid … Web6 de jun. de 2024 · Best answer O 2 NCH 2 CH 2 O– is more stable than CH 3 CH 2 O– because NO 2 group has –I effect and hence it tends to disperse the negative charge on the oxygen atom. In contrast, CH 3 CH 2 has +I effect. It, therefore, tends to intensify the negative charge and hence destabilizes it. ← Prev Question Next Question → Find …
Web13 de abr. de 2024 · Expert Answer 1) O 2 NCH 2 CH 2 O - : Nitro group is an electron-withdrawing group which show -I effect, this effect allows the withdrawing of electrons … Web6 de jun. de 2024 · Best answer O 2 NCH 2 CH 2 O– is more stable than CH 3 CH 2 O– because NO 2 group has –I effect and hence it tends to disperse the negative charge on …
WebQuestion 12.9: Which of the two: O2NCH2CH2O– or CH3CH2O– is expected to be more stable and why? Answer: NO2 group is an electron-withdrawing group. Hence, it shows –I effect. By withdrawing the electrons toward it, the NO2 group decreases the negative charge on the compound, thereby stabilising it. 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 …
WebO2NCH2CH2O- is more stable than CH3CH2O- because NO2 has I-effect and hence, it tends to disperse the negative charge on oxygen atom. CH3CH2 exerts a +Ieffect and it tends to intensify the negative charge and destabilize it. Question 12.10 Explain why alkyl groups act as electron donors when attached to a π system.
WebNitroethoxide ion is more stable than ethoxide ion due to -I effect of nitro group which decreases the negative charge of oxide ion of nitroethoxide ion leading to stability. getshinearmor.comWebAnswer (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 , … get sherlockWebIdentify the functional groups in the following compounds: AnswerWhich of the two: O2NCH2CH2O or CH3CH2O is expected to be more stable and why? … Explain why alkyl groups act as electron donors when attached to a π-system. Answer: Due … See full list on learncbse.in › Estimated Reading Time: 9 mins 1. get shelter the snowWebOn the other hand, ethyl group is an electron-releasing group. Hence, the ethyl group shows +I effect. This increases the negative charge on the compound, thereby destabilising it. … gets highly theoreticalWebCH3 H3C+CH3 CH2 CH2 CH3 is more stable than HycCH3, because (A) carbocation stability doesn't depend on resonance effect (B) in the former phenyl is -IE group while in the later the substituted phenyl is stronger -IE group (C) in the later resonance stabilization is inhibited (D) carbocations are less stable when the molecule is bulky 1 1 gets higher crosswordWeb21 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 … christmas wish monoline fontget shift codes