Why do pengiuns have beards
2 answers:
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Answer:
3.38%
Explanation:
Given that;
the mass of the whole milk sample = 100 g
volume of HCl = 100 mL = 0.1 L
molarity of HCl = 0.5 M
volume of NaOH = 34.50 mL = 0.0345 L
molarity of NaOH = 0.3512 M
Since we knew the molarity and volume of both HCl and NaOH; we can calculate their corresponding number of moles present.
So, number of moles of HCl = molarity of HCl × volume of HCl
number of moles of HCl = 0.5 M × 0.100 mL
= 0.05 mole
number of moles of NaOH = Molarity of NaOH × Volume of NaOH
number of moles of NaOH = 0.3512 M × 0.0345 L
= 0.012 mole
From the question, we can deduce that the number of HCl that is consumed by NH₃ is equal to the number of moles of HCl that is consumed by NaOH.
SO, number of moles of HCl consumed by NH₃ = Total moles of HCl - moles of HCl consumed by NaOH
= 0.05 mole - 0.012 mole
= 0.038 mole
However, to determine the mole of NH₃ present , we have:
number of moles of NH₃ present = number of moles of HCl consumed by NH₃ = 0.038
∴ the mass of Nitrogen with the molecular weight (14.0 g/mol) = 0.038 moles × 14.0 g/mol
= 0.530 g
Now, the percentage of Nitrogen can be calculated as;
%
the percentage of protein in the sample = CP × %age of N
where CP is given as 6.38
∴ the percentage of protein in the sample = 6.38 × 0.530%
the percentage of protein in the sample = 3.3814%
the percentage of protein in the sample = 3.38%
Answer:
See explanation
Explanation:
The reaction that we are considering here is quite a knotty reaction. It is difficult to decide if the mechanism is actually E1 or E2 since both are equally probable based on the mass of scientific evidence regarding this reaction. However, we can easily assume that the methylenecyclohexane was formed by an E1 mechanism.
Looking at the products, one could convincingly assert that the reaction leading to the formation of the two main products proceeds via an E1 mechanism with the formation of a carbocation intermediate as has been shown in mechanism attached to this answer. Possible rearrangement of the carbocation yields the 3-methylcyclohexene product.
