Answer:
The product is cyclohexanol
Explanation:
Firstly,
A ketone undergo a borohydride reduction reaction to form an alcohol as below,
R-CO-R' ⇒ R-CO(OH)-R'
- IR Spectrum confirms that alcohol group is existed with the peak at 3400 cm⁻¹
- From 1H-NMR, the product has 10 hydrogen atoms, the MS suggest that the formula is C₅H₁₀O (M = 86). With this formula, the alcohol is monosaturated. Since, the substance already underwent reduction reaction, the only way to suggest a monosaturated compound is a cyclic alcohol. So the compound is cyclopentanol.
- Check with other spectroscopic properties,
- 3 signals of 13C NMR confirms the structure is symmetrical, δ 24.2, (-<u>C</u>H₂-CH₂-CH(CH₂-)-OH), δ 35.5 (-CH₂-<u>C</u>H₂-CH(CH₂-)-OH), δ 73.3 (-CH₂-CH₂-<u>C</u>H(CH₂-)-OH).
1.56 δ (4H, triplet) - (-C<u>H</u>₂-CH₂-CH-OH) ; triplet as coupling with 2 H,
1.78 δ (4H, multiplet) - (-CH₂-C<u>H</u>₂-CH-OH); multiplet as coupling with 2H of CH₂, 1 H of CH
3.24 δ (1H, quintet); - (-CH₂-CH₂-C<u>H</u>(CH₂-)-OH), coupling with4 H of 2 group of CH₂
3.58 δ (1H, singlet); - (-CH₂-CH₂-CH(CH₂-)-O<u>H</u>), hydrogen of alcohol group, not tend to coupling with other hydrogen
RbOH is a strong base that dissociates completely and HCl is a strong acid that too dissociates completely. the complete reaction between the acid and base is;
RbOH + HCl ---> RbCl + H₂O
stoichiometry of acid to base is 1:1
At neutralisation point
H⁺ mol = OH⁻ mol
mol = molarity x volume
if Ma - molarity of acid and Va - volume of acid reacted
Mb - molarity of base and Vb - volume of base reacted
Ma x Va = Mb x Vb
0.5 M x 52.8 mL = Mb x 60.0 mL
Mb = 0.44 M
molarity of base - 0.44 M
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We assume that we have Ka= 4.2x10^-13 (missing in the question)
and when we have this equation:
H2PO4 (-) → H+ + HPO4-
and form the Ka equation we can get [H+]:
Ka= [H+] [HPO4-] / [H2PO4] and we have Ka= 4.2x10^-13 & [H2PO4-] = 0.55m
by substitution:
4.2x10^-13 = (z)(z)/ 0.55
z^2 = 2.31x 10^-13
z= 4.81x10^-7
∴[H+] = 4.81x10^-7
when PH equation is:
PH= -㏒[H+]
= -㏒(4.81x10^-7) = 6.32