
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. ...
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 ...
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 ...
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.
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
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 ...
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.
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).
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).
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.