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Question#1

Grignard reagent on reaction with acetone forms [BHU 1995; RPMT 2002; Roorkee 1990]

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Question#2

An alkene of molecular formula C9H18 on ozonolysis gives 2,2 dimethyl propanal & 2-butanon, then the alkene is [Kerala CET 2005]

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Question#3

When a mixture of methane and oxygen is passed through heated molybdenum oxide, the main product formed is [KCET 2004]

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Question#4

Ethyne on reaction with water in the presence of HgSO4 and H2SO4 gives [UPSEAT 1999; BVP 2003]

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Question#5

O3 reacts with CH2 =CH2 to form ozonide. On hydrolysis it forms [MP PET 1986, 90]

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Question#6

Hydrolysis of ozonide of 1-butene gives [Kerala PMT 2003]

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Question#7

Propyne on hydrolysis in presence of HCl and HgSO4 gives [DPMT 1980]

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Question#8

CH3- CO-CH3 can be obtained by [CBSE PMT 1992]

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Question#9

Methyl ethyl ketone is prepared by the oxidation of [IIT-JEE 1987; MP PMT 1992]

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Question#10

Which of the following compound gives a ketone with Grignard reagent [CPMT 1988; MP PET 1997]

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Question#11

On heating calcium acetate and calcium formate, the product formed is [DPMT 1984; EAMCET 1985; MP PMT 1996, 92; KCET 1990; CPMT 1979, 82, 84; BIT 1992; RPET 2000]

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Question#12

Acetophenone is prepared by the reaction of which of the following in the presence of AlCl3 catalyst[AIIMS 1996]

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Question#13

Dry heating of calcium acetate gives [DPMT 1979, 81, 96; NCERT 1981; KCET 1993; Bihar CEE 1995; MNR 1986; MP PMT 1997; MP PET 1993, 95; JIPMER 2002; AIIMS 1996; CPMT 1982, 86, 96, 2003; RPMT 2002]

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Question#14

\( CH_3-CH_2-C \equiv CH \xrightarrow[R]{H2O} Butanone \) , R is [BHU 2003]

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Question#15

The end product in the following sequence of reaction is [Bihar CEE 2002]

\( CH \equiv CH \xrightarrow[ HgSO4]{ H2SO4} A \xrightarrow[H2O]{CH3MgBr} B \xrightarrow{[O]} ?  \) 

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Question#16
Which of the following compounds will react with methyl magnesium Iodide followed by acid hydrolysis to give ethyl alcohol? (ETEA2014 ETEA2019)
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Question#17

formalin is an aqueous solution of NUMS2017 

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Question#18
A student mixed ethyl alcohol with small proportion of sodium dichromate and added it into the hot solution of dilute sulphuric acid. a vigorous reaction took place. he distilled the product immediately. What was the product? MDCAT2014
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Question#19

Na2Cr2O7 what the product will be when secondary alcohols are oxidized in same condition MDCAT2011

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Question#20

Dry distillation of calcium salt of acetic acid and formic acid results into formation of MDCAT2010

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Question#21

In the conversion of ethylene into acetaldehyde, cupric chloride acts as MDCAT2009

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Question#22

Aldehyde can be synthesized by the oxidation of MDCAT2008

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Question#23
What is the structure of alcohol which on oxidation with acidified Na2Cr2O7 gives C6H5-CO-CH3.  MDCAT2013
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Categories
1.    Introduction To Fundamental
         Atomic Mass
         Empirical formula
         Molecular Formula
         Concept of Mole
         Stoichiometry
         Limiting Reactant
         Percentage yield
2.    Atomic Strcuture
         Constituents of atom
         Properties of canal rays
         Rutherford Model
         Planks Theory
         Spectrum
         Bohr Model
         Hydrogen Spectrum
         de Broglie relation
         Uncertainty principle
         Quantum Number
         Electronic configuration
4.    Liquids
         Intermolecular forces
         hydrogen Bonding
         Evaporation
         Vapor Pressure
5.    Solids
         Types of Solids
         Ionic Solids
         Covalent Solids
         Molecular Solids
         Metallic solids
         Unit Cell
         Crystal System
7.    Reaction kinetics
10.    chemical Bonding
         Valency
         Octate Rule
         Ionization Energy
         Electron affinity
         Electronegativity
         Ionic Bond
         Covalent Bond
         Polarization
         Coordinate covalent Bond
         Sigma and pi Bond
         Hydrogen Bond
         VSEPR theory
         VBT
         Hybridization
         MOT
         Dipole moment
14.    Chemistry Of Hydrocarbons
17.    Alkyl halides
         IUPAC system
         SN1 & SN2
         E1 & E2
         Nucleophile and Base
20.    Macromolecules