Answer:
Isopropyl propionate
Explanation:
1. Information from formula
The formula is C₆H₁₂O₂. A six-carbon alkane would have the formula C₆H₁₄. The deficiency of two H atoms indicates the presence of either a ring or a double bond.
2. Information from the spectrum
(a) Triplet-quartet
A 3H triplet and a 2H quartet is the classic pattern for a CH₃CH₂- (ethyl) group
(b) Septet-doublet
A 1H septet and a 6H doublet is the classic pattern for a -CH(CH₃)₂ (isopropyl) group
(c) The rest of the molecule
The ethyl and isopropyl groups together add up to C₇H₁₂.
The rest of the molecule must have the formula CO₂ and one unit of unsaturation. That must be a C=O group.
The compound is either
CH₃CH₂-COO-CH(CH₃)₂ or (CH₃)₂CH-COO-CH₂CH₃.
(d) Well, which is it?
The O atom of the ester function should have the greatest effect on the H atom on the adjacent carbon atom.
The CH of an isopropyl is normally at 1.7. The adjacent O atom should pull it down perhaps 3.2 units to 4.9.
The CH₂ of an ethyl group is normally at 1.2. The adjacent O atom should pull it down to about 4.4.
We see a signal at 5.0 but none near 4.4. The compound is isopropyl propionate.
3. Summary
My peak assignments are shown in the diagram below.
Answer:I think this is right: 1. 6 2. 12 3. 4 4. In the middle 5. Carbon 1. The one on the right 2a. Beryllium 2b. Aluminium
Explanation:The protons are the circles with plus signs and the black ones are nutrons. I looked on my periodic table for the rest.
Answer:
A. Molarity will increase .
Explanation:
Molarity = moles of solute per litre of solution
= moles of solute / volume of solution
If evaporation occurs , volume of solution decreases and moles of solute remains constant . Hence denominator decreases and numerator remains constant .
Hence the molarity increases .
there is no conversion between the two due to one is time and one is weight
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