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
So in your question that ask to calculate the Ph result of the resulting solution if 26 ml of 0.260 M HCI(aq) is added to the following substance. The the result are the following:
A. The result is pH= 14-pOH
B. There are 10ml of 0.26m HCL excees in this reaction so the answer is log(H)+
<span>In chemistry, a catalyst can speed up the reaction (or make it initiate easier) by altering the activation energy, lowering it enough to allow the reactants to react more easily. Some negative catalysts or inhibitors can do the same by increasing the activation energy.
</span>
1a. calcium chloride (CaCl2)
b. 2HCl (aq) + Ca(OH)2 (s) —> CaCl2 (aq) + 2H2O (l)
i’m not sure about the rest but i hope this helped ^^