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1,1,1-trichloro-2-propanone

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Waldo Ledner

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3y ago

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What happens when sodium reacts with ethanol?

Sodium reacts with Ethanol to produce Sodium Ethoxide (C2H5ONa) and Hydrogen gas (H2), according to the following equation.2 C2H5OH + 2Na ----> 2 C2H5ONa + H2


CH3 plus CH3CH2OH what is the expected product?

The reaction between CH3 and CH3CH2OH (ethanol) is a radical substitution reaction. The expected product would be ethane (CH3CH3) and a ethoxy radical (CH3CH2O•).


What is zinc ethanoate?

Zinc ethanoate is a chemical compound with the formula Zn(C2H3O2)2. It is a white crystalline solid that is commonly used as a catalyst in organic reactions and as a corrosion inhibitor.


What is C2H5O?

C2H5O represents the molecular formula of ethoxy group, which consists of two carbon atoms, five hydrogen atoms, and one oxygen atom. It is commonly found in organic compounds and can be a part of various functional groups in organic chemistry.


How many hydrogen atoms in 2CH3CH2O?

2xH3 is 6 and 2xH2 is 4, therefore 10. Though CH3CH2O is not a molecule that exists (at least not anywhere near stably).


What happens if you mix alcohol and magnesium?

Mixing alcohol with magnesium can potentially cause irritation to the stomach lining, leading to symptoms such as nausea, vomiting, and stomach pain. Combining alcohol with magnesium supplements may also increase the risk of dehydration and magnesium toxicity. It is important to avoid combining the two substances and to consult a healthcare professional before taking any new supplements or medications while consuming alcohol.


Why phenol more acidic than alcohols?

Acidity depends on the concentration of H+. Due to higher electronegativity of sp2 hybridised carbon of phenol, the electron density on the oxygen decreases and hence increases the polarity O-H making the phenol unstable compared to phenolate, so it is more acidic. The C6H5-group is a fully sp2-hybridised electron pulling group.If you have electron providing groups (sp3) in CH3-CH2-O-H, it may decrease the polarity of O-H bond and destabilize the negatively charged ethanoate group (CH3CH2O-)


Is C2H5OH an electrolyte?

Organic molecules are typically considered to be terrible electrolytes (molecules that dissociate into ions). Because of strong covalent bonds, organics usually stick together. So the answer is "no".


What is a stonger base among methanthiolm and methanol?

Between methanethiol and methanol (if both species remain PROTONATED), I think methanethiol is the better base (ie, it is easier to form CH3CH2SH2+ than to form CH3CH2OH2+) because the lone pairs on the O are closer to the nucleus (O is more electronegative than S), so the O lone pairs are less available to reach out and grab a proton (aka they are less basic).Between the DEPROTONATED forms, methoxide (CH3CH2O-) is definitely more basic than methanethiolate (CH3CH2S-). ?Methanol has a higher pKa than methanethiol by about 5 pH units).


What is the structural formula for ethanol?

ethanol and waterEthanol = C2H6O or CH3CH2OH as is more accurate to its structure. Water = H2OWater and Ethanol, when mixed together, will do almost nothing. However, about 10^-14 %of the time water will react with itself to form H3O(+) and OH(-). At this point the OH(-) will capture the loosely bound Hydrogen from an ethanol molecule. The resulting equation looks like this.CH3CH2OH + H3O(+) + OH(-) = CH3CH2O(-) + H3O(+) + H2Owhere the sign in parenthesis is the formal charge for the molecule. Remember, this only happens around 10^-14 % of the time and is very difficult to measure or even separate from the solution. Most of the time water and ethanol will not react and you'll simply get wet ethanol.


Why alcohols are more acidic than ammonia?

Phenols are much more acidic than alcohols. This is indicated in the order of acidity constant:Ka Gernal formulaPHENOLS 10-10 Ar-OHALCOHOLS 10-18 C-OHPhenols are more acidic due to the formation of phenoxide ions & phenoxide ions are stable due to resonance, the negative charge on oxygen is spread throughout the benzene ring & is delocalised. On the other hand no resonance is possible in alkoxide ions derived from alcohol. The negative charge is localised on single oxygen atom.


What is meant by conjugate base and acid?

The acid formed when a base gains an H+