MARAN ACADEMY
PG TRB CHEMISTRY
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- .
Allenes show optical activity because of the presence of- chiral carbon atom
- conjugated double bond
- isolated double bond
- cumulated double bond
- A molecule which is optically active
- is asymmetric as a whole
- contains at least three chiral centres
- is super imposable on its mirror image
- must be a meso compound
- Enantiotropic groups react with chiral reagents
- at different rate
- at the same rate
- same rate at the first and different rates later
- do not react at all
- .
Which of the following definitions of an asymmetric reaction is the most accurate?- A reaction that creates a new chiral centre in the product
- A reaction that involves a chiral reagent
- A reaction that is carried out on an asymmetric starting material
- A reaction that is carried out on an asymmetric starting material Enantiotropic
groups react with chiral reagents
- What is meant by a reaction going in 94% enantiomeric excess?
- The product contains 94% of one enantiomer and 6% of the other enantiomer
- The product contains 94% of one enantiomer and 6% of other products
- The product contains an enantiomer which is 94% pure.
- The product contains 97% of one enantiomer and 3% of the other enantiomer
- .
Two optical isomers are formed from carbon atoms to create bond- 4 atoms
- 1 atoms
- 2 atoms
- 3 atoms
- Stereoisomers that arise from restricted rotation about a single bond can be
- Enantiomers
- Diasteriosmers
- Atropisomers
- Epimers
- Example of compound having axial chirality is
- Allene
- Compounds having asymmetric carbon
- Meso Compounds
- erytreo compounds
- .
Asymmetric synthesis can be done using- Anthraquinone
- Quinoline
- Benzaldehyde
- Emulsin
- Antifungal drug Mycomycin is a ------ derivative
- Allene
- Spirane
- Biphenyl
- Ansa
- .
The most stable conformation of Butane is- skew conformations
- gauche conformations
- eclipsed conformations
- Anti conformations
- A cisoid arrangement means to
- eclipsed conformations
- anti staggered conformations
- skew conformations
- gauche conformations
- .
The most unstable conformation of cyclohexane is- chair
- half chair
- wist-boat
- boat
- .
In the complete rotation of butane from 0 degree to 360 degree the gauche-staggered conformation appears- once
- twice
- thrice
- four times
- .
Trans bromine addition to cis-2-butene yields- D-2, 3-dibromobutane
- l-2, 3-dibromobutane
- racemic-2, 3-dibromobutane
- meso-2, 3-dibromobutane
- The conformation of cyclohexane which is free from all strain is
- chair
- half chair
- twist
- boat
- . α- D (+) glucose and β- D (+)glucose are
- Enantiomers
- Diastereomers
- Epimers
- Anomers
- .
Which cycloalkane has the greatest ring strain?- Cyclopropane
- Cyclobutane
- Cyclopentane
- Cyclohexane
- In the most stable conformation of cis-1,4-dimethylcyclohexane, the methyl groups are:
- both equatorial
- both axial
- one axial, one equatorial.
- None of the above.
- .
The twist boat conformation is the preferred conformation for this compound.- trans-1,4-Di-tert-butylcyclohexane
- cis-1,4-Di-tert-butylcyclohexane
- trans-1,2-Di-tert-butylcyclohexane
- cis-1,3-Di-tert-butylcyclohexane
- .
The Reformalsky reaction is often used for the preparing of- α-hydroxy ester
- β-hydroxy ester
- α-halo ester
- β-halo ester
- Ethyl acetoacetate is prepared from ethyl acetate by
- Claisen condensation
- Reformalsky reaction
- Aldol condensation
- Perkin reaction
- Which of the following reaction undergoes the Grignard like reaction?
- Aldol condensation
- Reformalsky reaction
- Wittig reaction
- Perkin reaction
- .
Coumafin is prepared industrially from salicylaldehyde by- Stobbe reaction
- Reformatsky reaction
- Wittig reaction
- Perkin reaction
- In case of cyclic dienes the Diels-Alder reaction gives the end product exclusively at
- low temperature
- high temperature
- all temperatures
- at 0 degree celcius
- Usually Diels-Alder reaction is
- 4 + 2 cyclo addition
- 2 + 2 cyclo addition
- 2 + 4 cyclo addition
- none of the above
- Esterification is quick in ------medium
- Basic
- Acidic
- Neutral
- Non polar
- Aldehydes with lack of α-hydrogen undergoes disproportion reaction is
- Wittig reaction
- Reformatsky reaction
- Cannizaro reaction
- Perkin reaction
- .
The Claisen condensation is often used in preparing- β-hydroxy ester
- β- keto ester
- γ-keto ester
- α-hydroxy ester
- The intermediate formed in E1CB mechanism is
- Carbonium ion
- Depends on substrate
- Carbanium
- Free radical