About: Diethyl Ether   Sponge Permalink

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A nucleophilic oxygen atom of unprotonated ethanol displaces a water molecule from the protonated (electrophilic) ethanol molecule, producing water, a hydrogen ion and diethyl ether. CH3CH2OH2+ + CH3CH2OH → H2O + H+ + CH3CH2OCH2CH3

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  • Diethyl Ether
  • Diethyl ether
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  • A nucleophilic oxygen atom of unprotonated ethanol displaces a water molecule from the protonated (electrophilic) ethanol molecule, producing water, a hydrogen ion and diethyl ether. CH3CH2OH2+ + CH3CH2OH → H2O + H+ + CH3CH2OCH2CH3
  • Custom element Japanese name: (ジエチルエーテル) Jiechiruēteruton Custom element English name: Diethyl Ether The element is based on: (Wind + Earth + Lightning )+ Chakra Facts that prove the element to be possible (in the manga context): In Naruto, we have seen that there are clouds which are capable of raining down oil and a mist that is capable of igniting fire as well. Ether has the same chemical reaction to fire as oil, but can also be used as a drug/anesthetic in either it's liquid or Mist/vapor/gaseous state. For liquid ether, if swallowed by an opponent, it affects their mind and body, making the opponent act in a drunken like state. Their actions are all severely lowered; reaction, reflexes, balance and clouds their judgment and thought process. In its gaseous state, Ether, when inhaled, h
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abstract
  • Custom element Japanese name: (ジエチルエーテル) Jiechiruēteruton Custom element English name: Diethyl Ether The element is based on: (Wind + Earth + Lightning )+ Chakra Facts that prove the element to be possible (in the manga context): In Naruto, we have seen that there are clouds which are capable of raining down oil and a mist that is capable of igniting fire as well. Ether has the same chemical reaction to fire as oil, but can also be used as a drug/anesthetic in either it's liquid or Mist/vapor/gaseous state. For liquid ether, if swallowed by an opponent, it affects their mind and body, making the opponent act in a drunken like state. Their actions are all severely lowered; reaction, reflexes, balance and clouds their judgment and thought process. In its gaseous state, Ether, when inhaled, has no real visible effect at first. However, a person who inhales it will not feel pain, which, if done on purpose (self administered) is a good thing, as it would allow you to feel less pain than what you normally would, but you would have a conscience mind not to push your body over the limit. When it is given to you without your knowledge, you don't know that you can't push your body the way you normally would, and therefore will suffer the consequences of it. If inhaled for over a period of time, numbness will restrict your mind, and cause loss of consciousness. Idea behind its creation: I wanted to create an element that had duel effects to a person. Not necessarily one that would cause physical harm to them, but could affect them and their chakra system or their body's natural reaction or way of doing things. Also, Ether is very flammable, which makes it a good element to be scared of, being stronger than a mere Wind/Fire Combination. Also known as ethyl ether, simply ether, or ethoxyethane, is an organic compound in the ether class with the formula (C2H5)2O. It is a colorless, highly volatile flammable liquid with a characteristic odor. It is commonly used as a solvent and was once used as a general anesthetic. Ether is sparingly soluble in water.
  • A nucleophilic oxygen atom of unprotonated ethanol displaces a water molecule from the protonated (electrophilic) ethanol molecule, producing water, a hydrogen ion and diethyl ether. CH3CH2OH2+ + CH3CH2OH → H2O + H+ + CH3CH2OCH2CH3 This reaction must be carried out at temperatures lower than 150 °C in order to ensure that an elimination product (ethylene) is not a product of the reaction. At higher temperatures, ethanol will dehydrate to form ethylene. The reaction to make diethyl ether is reversible, so eventually an Chemical equilibrium between reactants and products is achieved. Another reaction that can be used for the preparation of ethers is the Williamson ether synthesis, in which an alkoxide (produced by dissolving an alkali metal in the alcohol to be used) performs a nucleophilic substitution upon an alkyl halide.
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