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  1. Which one is the stronger nucleophile? CH3CH2O or CH3CO2

    Apr 30, 2020 · CH3CH2O or CH3CO2 [closed] Ask Question Asked 4 years, 11 months ago. Modified 4 years, 11 months ago. ...

  2. What is CH3CH2O? - Answers

    May 23, 2024 · CH3CH2O is the chemical formula for ethyl methyl ether, which is an organic compound that is also known as methoxyethane. It is a colorless liquid with a sweet odor, commonly used as a solvent or ...

  3. What is the common name of ch3ch2 o ch2ch3? - Answers

    Jun 29, 2024 · This always depends on where you place the -OH group, though usually this is called Propanol or Propan-1-ol This always depends on where you place the -OH group, though usually this is called ...

  4. How many atoms are in CH3CH2OH? - Answers

    May 30, 2024 · There are 9 atoms in CH3CH2OH: 2 carbon atoms, 6 hydrogen atoms, and 1 oxygen atom.

  5. What are the products formed when CH3CH2OH reacts with NaH?

    May 16, 2016 · There are a number of reasons why the reaction you suggest in much less favourable than the deprotonation. Firstly, hydride is a terrible nucleophile because its 1s orbital is too small to effectively overlap with anything except hydr

  6. How to tell/control whether sodium ethoxide will react by a ...

    Mar 29, 2018 · Exceptions: (a) Bulky bases such as $\ce {(CH3)3CO-}$ (note that $\ce {CH3CH2O-}$ is not considered to be 'bulky') gives E2 product predominantly; and (b) some primary halides such as allyl and benzyl halides can form relatively stable carbocations (by resonance stabilization, for example) may proceed through either of S N 2, S N 1, or E1 ...

  7. Determine if an acid base reaction will occur

    Apr 24, 2016 · $$\ce{ch3ch2oh + h2o <<=> ch3ch2o- + h3o+}$$ Why does this reaction occur, because the alkoxide ion is a really strong base right? Why should its conjugate acid give off a $\ce{H+}$ to water, if it was a strong base let's say $\ce{NaOH}$ it would make sense to me, because the $\ce{OH-}$ is probably a stronger base then the alkoxide ion.

  8. Is ethanol an acid or a base or amphoteric? - Chemistry Stack …

    Apr 17, 2017 · Because we are talking about Brønsted–Lowry acids and bases, we are only concerned with whether or not a molecule has (or the degree to which it has) the ability to donate a proton (acid) or the ability to accept a proton (base) or to do either (amphoteric).

  9. Who makes a better nucleophile? CH3O- or OH-? [duplicate]

    Aug 16, 2021 · When the donor atom is same, a general rule applies: nucleophilicity parallels basicity. Thus, comparing the basic strength of methoxide and hydroxide, it is observed that methoxide is a stronger base than hydroxide (as it the conjugate base of a weaker acid i.e. methanol when compared to water).

  10. organic chemistry - Nucleophilicity order in polar protic solvent ...

    Apr 27, 2024 · $\ce{CH3CH2O-}$ has maximum charge density. $\ce{CH3COO-}$ will have more charge density than $\ce{CH3CH2S-}$ but less than $\ce{CH3CH2O-}$ as it is resonance stabilised. Therefore order of nucleophilicity should be $\pu{(1>3>2)}$. But in the answer key, $\pu{(1>2>3)}$ is the right answer.

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