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MrRissso [65]
3 years ago
11

Hydration of alkynes gives good yields of single compounds only with symmetrical or terminal alkynes. Draw the major organic pro

duct(s) formed when 3-methylcyclodecyne undergoes hydration in the presence of HgSO4 and H2SO4.
Chemistry
1 answer:
Alexxandr [17]3 years ago
8 0

Answer:

Following are the solution to the given choice:

Explanation:

Hex-2-yne is just not alkyne symmetric, therefore two things respectively hexan-3-one and hexan-2-one are to be given.

The attached file it displayed the response along with the mechanism, please find the.

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The molecular formula of the unknown compound is determined as  C₉H₁₁NO₂.

<h3>Molecular formula of the compound</h3>

The molecular formula is calculated as follows;

CHNO  +  O₂ ------------> CO₂  + H₂O

Mass of carbon, C:  = (6.64 x 12)/44 = 1.81 g in 2.77 g sample

Mass of hydrogen, H: = (1.67 x 2)/18 = 0.186 g in 2.77 g sample

Mass of Nitrogen, N: = (2.77 x 0.143)/1.69 = 0.234 g

Mass of oxygen, O:  = 2.77 g - 1.81 g - 0.186 g - 0.234 g = 0.54 g

<h3>molar ratio of the elements: </h3>

C = 1.81 g = 0.15 mol

H = 0.186 g = 0.186 mol

N = 0.234 g = 0.017 mol

O = 0.54 g = 0.0337 mol

divide through with the smallest number of moles (0.017 mol);

C = 9

H = 11

N = 1

O = 2

Molecular formula = C₉H₁₁NO₂

Check the molar mass of the compound = (9 x 12) + (11 x 1) + (14) + (2 x 16) = 165 g/mol

Thus, the molecular formula of the unknown compound is determined as  C₉H₁₁NO₂.

Learn more about molecular mass here: brainly.com/question/21334167

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