Which proton(s) in methyl salicylate are responsible for the resonance at 10.7 ppm? Which are responsible for the resonance at 3.9 ppm?
Methyl salicylate is also called methyl 2-hydroxy benzoate. The structure is as follows.
As shown in the figure above, , the proton belongs to –OH appears at 10.7 ppm and the proton belongs to –COOCH3 appears at 3.9 ppm in the HNMR spectrum of methylsalicylate.
Which proton(s) in methyl salicylate are responsible for the resonance at 10.7 ppm? Which are responsible for the resonance at 3.9 ppm?
1.Which protons in methyl salicylate are resonsible for the
resonance at 10.7 ppm? Which are responsible forthe resonance at
3.9 ppm?
2. Which carbon in methyl salicylate is respocsible for the
resonance at 170.6 ppm? Which is responsible for the resonance at
52.2 ppm?
3. In the aromatic area of the proton NMR of methyl salicylate
there is a doublet at 7.81 ppm. Which aromatic proton in the
structure is responsile for this resonance?
4. What is the major new...
In the aromatic area of the proton NMR of methyl salicylate there is a doublet at 7.81 ppm. Which aromatic proton in the structure is responsible for this resonance?
Which carbon in methyl salicylate is responsible for the resonance at 170.6 ppm? Which is responsible for the resonance at 52.2 ppm?
1. In the H NMR of benzaldehyde, which proton is responsible for
the resonance at 10.0 ppm? In the aromatic area there are three
sets of multiplets at 7.87, 7.61 and 7.51 that integrte for 2:1:2
protons respectively. Which protons are responsible for these
multiplets?
In the C NMR of benzaldehyde, which carbon is responsible for
the resonance at 192 ppm?
NMR Spectra H and C spectra of benzaldehyde and benzoin are shown below. CDCl 240 QE-300 180 220 160...
What carbons in acetylsalicylic acid are responsible for the resonances at 170.2 and 169.8 ppm? Which carbon is responsible for the resonance at 20.9 ppm? Which four carbons are responsible for the large peaks at 134.9, 132.5, 126.2 and 124.0 ppm?
Which carbon is responsible for the resonance at 172.2 ppm in the NMR of salicylic acid?
In the 13C NMR of isoamyl alcohol, which carbon is responsible for the resonance at 60.9 ppm? Which carbons are equivalent (give one signal) in the 13C NMR of isoamyl alcohol?
Question 1 What is the mechanism of the synthesis of methyl salicylate? esterification Sn1 SnAcyl AnE Question 2 Which compound is responsible for the burnt-fat odor in the test for glycerol? glycerol acrolein acetic acicd o fatty acid Question 3 Which of the following reagents is NOT used for the synthesis of methyl salicylate? o acetic acid methanol salicylic acid sulfuric acid Question 4 Which of the following chemically define a soap? salt of a thoester salt of a carboxylic...
In the H1 NMR of isoamyl acetate, which protons are responsible for the triplet at 4.1 ppm? Which protons are responsible for the doublet at 0.93 ppm?
Which two reactants are used to form methyl salicylate? Сн, он HO-CH2CH2CH2CH2CH3 Оно-СН3