Reaction of 2-methylpropanoic acid [ ( CH 3 ) 2 CHCO 2 H ] with SOCl 2 followed by 2-methylpropan-1-ol forms X . X has a molecular ion at 144 and IR absorptions at 2965, 2940, 1739 cm − 1 . Propose a structure for X .
Reaction of 2-methylpropanoic acid [ ( CH 3 ) 2 CHCO 2 H ] with SOCl 2 followed by 2-methylpropan-1-ol forms X . X has a molecular ion at 144 and IR absorptions at 2965, 2940, 1739 cm − 1 . Propose a structure for X .
Solution Summary: The author explains the possible structure of X. The molecular ion is formed by ejection of electrons from a molecule.
Reaction of 2-methylpropanoic acid
[
(
CH
3
)
2
CHCO
2
H
]
with
SOCl
2
followed by 2-methylpropan-1-ol forms
X
.
X
has a molecular ion at
144
and IR absorptions at
2965, 2940, 1739 cm
−
1
. Propose a structure for
X
.
Reaction of 2-methylpropanoic acid [(CH3)2CHCO2H] with SOCl2 followed by 2-methylpropan-1-ol forms X. X has a molecular ion at 144 and IR absorptions at 2965, 2940, and 1739 cm-1. Propose a structure for X.
Treatment of benzoic acid (C6H5CO2H) with NaOH followed by 1-iodo-3methylbutane forms H. H has a molecular ion at 192 and IR absorptions at 3064, 3035, 2960−2872, and 1721 cm−1. Propose a structure for H.
A solution of acetone [(CH3)2C=O] in ethanol (CH3CH2OH) in the presence of a trace of acid was allowed to stand for several days, and a new compound of molecular formula C7H16O2 was formed. The IR spectrum showed only one major peak in the functional group region around 3000 cm−1, and the 1H NMR spectrum is given here. What is the structure of the product?
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