Answer:
Explanation:Here's li
nkly/3fcEdSx to the answer:
bit.
Answer:
Electrons are transferred between atoms together in the ionic compound. The ions are arranged in a regular repeating pattern in an ionic crystal
Explanation:
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
Hope this helps
Answer- 1 mole
The equation for the reaction is:
C₄H₈O₂ + C₂H₅OH = C₆H₁₂O₂ + H₂O
Now you see that the number of the moles of butanoic acid
and etyl butyrate is equal in
the reaction. That means;
number of moles of C₄H₈O₂ = number of moles of C₆H₁₂O₂
mass of C₄H₈O₂/ Molar mass of C₄H₈O₂ = mass of C₆H₁₂O₂/ molar mass of C₆H₁₂O₂
mass of C₆H₁₂O₂ = molar mass of C₆H₁₂O₂ x mass of C₄H₈O₂/ Molar mass of C₄H₈O₂
Now, assuming <span>100% yield, the mass
of ethyl butyrate produced is: </span>
<span>= 7.45/88.11 x 116.16</span>
<span>=9.82g</span>
<span>Thus, the theoretical yield of ethyl butyrate is 9.82g.</span>
