A compound with the molecular formula C₅H₁₀O₂ gave the following ¹H NMR spectrum: triplet,

\delta

0.90
Multiplet,

\delta

1.60
Singlet,

\delta

1.95
Triplet,

\delta

3.95
The IR spectrum showed a strong absorption band near 1740 cm^-1.The most likely structure for the compound is:
A)
$A compound with the molecular formula C5H10O2 gave the following 1H NMR spectrum: triplet, \delta 0.90 Multiplet, \delta 1.60 Singlet, \delta 1.95 Triplet, \delta 3.95 The IR spectrum showed a strong absorption band near 1740 cm-1.The most likely structure for the compound is: A) B) C) D) E)$
B)
$A compound with the molecular formula C5H10O2 gave the following 1H NMR spectrum: triplet, \delta 0.90 Multiplet, \delta 1.60 Singlet, \delta 1.95 Triplet, \delta 3.95 The IR spectrum showed a strong absorption band near 1740 cm-1.The most likely structure for the compound is: A) B) C) D) E)$
C)
$A compound with the molecular formula C5H10O2 gave the following 1H NMR spectrum: triplet, \delta 0.90 Multiplet, \delta 1.60 Singlet, \delta 1.95 Triplet, \delta 3.95 The IR spectrum showed a strong absorption band near 1740 cm-1.The most likely structure for the compound is: A) B) C) D) E)$
D)
$A compound with the molecular formula C5H10O2 gave the following 1H NMR spectrum: triplet, \delta 0.90 Multiplet, \delta 1.60 Singlet, \delta 1.95 Triplet, \delta 3.95 The IR spectrum showed a strong absorption band near 1740 cm-1.The most likely structure for the compound is: A) B) C) D) E)$
E)
$A compound with the molecular formula C5H10O2 gave the following 1H NMR spectrum: triplet, \delta 0.90 Multiplet, \delta 1.60 Singlet, \delta 1.95 Triplet, \delta 3.95 The IR spectrum showed a strong absorption band near 1740 cm-1.The most likely structure for the compound is: A) B) C) D) E)$

Which Compound Would Be Most Acidic