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Basics of Organic Reaction Mechanism
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Among the carboxylic acid shown below, the ones that exhibit stereoisomerism and also form, cyclic anhydrides on heating are
I. HOOCCH(CH3)CH2CH2COOH
II. HOOCCH(C3H7)COOH
III. HOOCCH(C2H5)CH2COOH
IV. HOOCC(CH3)(C2H5)COOH

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Match the following compounds with their respective classes
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The sequence of an mRNA molecule produced from a DNA template strand with the composition 5'-AGCTACACT-3' is

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Pyrrole + PhMgBr → E + F
E + MeCl → G + H
F + MeCl → no reaction without a catalyst
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The structure of products E - H respectively are

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The mono protonation of adenine (X) in acidic solution mainly occurs at
Basics of Organic Reaction Mechanism mcq question image

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The molecules(s) that exist as meso structure (s)
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is/are

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Three molecular ionic states, P-R are possible for the amino acid histidine. Identify the correct choice of pH values, respectively for the observation of the ionic states P-R.
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In allene, hybridization of the central and terminal carbons respectively, are

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Benzene cannot be iodinated with directly. However, in presence of oxidants such as HNO3, iodination is possible. The electrophiles formed in the case is

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In electrophilic aromatic substitution reactions, nitro group is meta-directing because the nitro group

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The major product formed in the reaction of anisole with lithium, liquid ammonia and t-butanol is

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The number of signals that appear in the broad-band decoupled 13C NMR spectrum of ortho, meta and para-dichlorobenzene, respectively are

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The configurations at the two asymmetric centres (C-1 and C-6) in the bicyclo [4.4.0] decane, given below are
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In the reaction,
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if the concentration of both the reagents is doubled then the rate of the reaction will

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Cyclohexyl benzyl ether when reacted with hydrogen in the presence of 10% palladium on charcoal generates a mixture of

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Optically active 2-octanol rapidly loses its optical activity when exposed to

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Benzaldehyde can be prepared by reacting phenyl magnesium bromide with

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The increasing order of basicity among the following is
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The major product (X) of the monobromination reaction is
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Proton decoupled 13C NMR spectrum of a bicyclooctane (C8H14), exhibits only two signals. The structure of the compound is

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