232251
The well known compounds, $(+)$ - lactic acid and (-)- lactic acid, have the same molecular formula, $\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}_{3}$. The correct relationship between them is
1 constitutional isomerism
2 geometrical isomerism
3 identicalness
4 optical isomerism
Explanation:
The correct relationship between (+) lactic acid and $(-)$ lactic acid is optical isomer because it has one assymmetric center is chiral center. Both are optical isomers because they rotate the plane of polarized light in opposite direction.
3 will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
4
Explanation:
, b, d) Exp:(A, B, D) : Tautomerism is exhibited by molecules containing one or more $\alpha$-hydrogens (c.) will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232253
An optically active compound having molecular formula $\mathrm{C}_{2} \mathrm{H}_{16}$ on ozonolysis gives acetone as one of the products. The structure of the compound is
1
2
3
4
Explanation:
In compound we know ozonolysis in the presence of $\mathrm{zn} / \mathrm{H}_{2} \mathrm{O}$ we get one compound as a ketone while in other we get other compound.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232257
The isomerisation of 1-butyne to 2- butyne can be achieved by treatment with
1 hydrochloric acid
2 ammoniacal silver nitrate
3 ammoniacal cuprous chloride
4 ethanolic potassium hydroxide
Explanation:
Isomerisation of 1-butyne to 2-butyne can be achieved by treatment with alcoholic $\mathrm{KoH}$. In the presence of alcoholic $\mathrm{KoH}$ it $\beta$-elimination. The isomerisation of 1-butyne to 2-butene can be also achieved by treatment with $\mathrm{NaNH}_{2}$ / liq. ammonia.
WB JEET-2017
GENERAL ORGANIC CHEMISTRY
232258
The conformations of n-butane, commonly known as eclipsed, gauche and anti-conformations can be interconverted by
1 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methyl group
2 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methylene group
3 rotation around $\mathrm{C} 1-\mathrm{C} 2$ linkage
4 rotation around $\mathrm{C} 2-\mathrm{C} 3$ linkage
Explanation:
The conformation of n-butane commonly known as eclipsed, gauche and anti-conformations can be achieved by rotation around $\mathrm{C}_{2}$ and $\mathrm{C}_{3}$ linkage
232251
The well known compounds, $(+)$ - lactic acid and (-)- lactic acid, have the same molecular formula, $\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}_{3}$. The correct relationship between them is
1 constitutional isomerism
2 geometrical isomerism
3 identicalness
4 optical isomerism
Explanation:
The correct relationship between (+) lactic acid and $(-)$ lactic acid is optical isomer because it has one assymmetric center is chiral center. Both are optical isomers because they rotate the plane of polarized light in opposite direction.
3 will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
4
Explanation:
, b, d) Exp:(A, B, D) : Tautomerism is exhibited by molecules containing one or more $\alpha$-hydrogens (c.) will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232253
An optically active compound having molecular formula $\mathrm{C}_{2} \mathrm{H}_{16}$ on ozonolysis gives acetone as one of the products. The structure of the compound is
1
2
3
4
Explanation:
In compound we know ozonolysis in the presence of $\mathrm{zn} / \mathrm{H}_{2} \mathrm{O}$ we get one compound as a ketone while in other we get other compound.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232257
The isomerisation of 1-butyne to 2- butyne can be achieved by treatment with
1 hydrochloric acid
2 ammoniacal silver nitrate
3 ammoniacal cuprous chloride
4 ethanolic potassium hydroxide
Explanation:
Isomerisation of 1-butyne to 2-butyne can be achieved by treatment with alcoholic $\mathrm{KoH}$. In the presence of alcoholic $\mathrm{KoH}$ it $\beta$-elimination. The isomerisation of 1-butyne to 2-butene can be also achieved by treatment with $\mathrm{NaNH}_{2}$ / liq. ammonia.
WB JEET-2017
GENERAL ORGANIC CHEMISTRY
232258
The conformations of n-butane, commonly known as eclipsed, gauche and anti-conformations can be interconverted by
1 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methyl group
2 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methylene group
3 rotation around $\mathrm{C} 1-\mathrm{C} 2$ linkage
4 rotation around $\mathrm{C} 2-\mathrm{C} 3$ linkage
Explanation:
The conformation of n-butane commonly known as eclipsed, gauche and anti-conformations can be achieved by rotation around $\mathrm{C}_{2}$ and $\mathrm{C}_{3}$ linkage
232251
The well known compounds, $(+)$ - lactic acid and (-)- lactic acid, have the same molecular formula, $\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}_{3}$. The correct relationship between them is
1 constitutional isomerism
2 geometrical isomerism
3 identicalness
4 optical isomerism
Explanation:
The correct relationship between (+) lactic acid and $(-)$ lactic acid is optical isomer because it has one assymmetric center is chiral center. Both are optical isomers because they rotate the plane of polarized light in opposite direction.
3 will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
4
Explanation:
, b, d) Exp:(A, B, D) : Tautomerism is exhibited by molecules containing one or more $\alpha$-hydrogens (c.) will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232253
An optically active compound having molecular formula $\mathrm{C}_{2} \mathrm{H}_{16}$ on ozonolysis gives acetone as one of the products. The structure of the compound is
1
2
3
4
Explanation:
In compound we know ozonolysis in the presence of $\mathrm{zn} / \mathrm{H}_{2} \mathrm{O}$ we get one compound as a ketone while in other we get other compound.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232257
The isomerisation of 1-butyne to 2- butyne can be achieved by treatment with
1 hydrochloric acid
2 ammoniacal silver nitrate
3 ammoniacal cuprous chloride
4 ethanolic potassium hydroxide
Explanation:
Isomerisation of 1-butyne to 2-butyne can be achieved by treatment with alcoholic $\mathrm{KoH}$. In the presence of alcoholic $\mathrm{KoH}$ it $\beta$-elimination. The isomerisation of 1-butyne to 2-butene can be also achieved by treatment with $\mathrm{NaNH}_{2}$ / liq. ammonia.
WB JEET-2017
GENERAL ORGANIC CHEMISTRY
232258
The conformations of n-butane, commonly known as eclipsed, gauche and anti-conformations can be interconverted by
1 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methyl group
2 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methylene group
3 rotation around $\mathrm{C} 1-\mathrm{C} 2$ linkage
4 rotation around $\mathrm{C} 2-\mathrm{C} 3$ linkage
Explanation:
The conformation of n-butane commonly known as eclipsed, gauche and anti-conformations can be achieved by rotation around $\mathrm{C}_{2}$ and $\mathrm{C}_{3}$ linkage
232251
The well known compounds, $(+)$ - lactic acid and (-)- lactic acid, have the same molecular formula, $\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}_{3}$. The correct relationship between them is
1 constitutional isomerism
2 geometrical isomerism
3 identicalness
4 optical isomerism
Explanation:
The correct relationship between (+) lactic acid and $(-)$ lactic acid is optical isomer because it has one assymmetric center is chiral center. Both are optical isomers because they rotate the plane of polarized light in opposite direction.
3 will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
4
Explanation:
, b, d) Exp:(A, B, D) : Tautomerism is exhibited by molecules containing one or more $\alpha$-hydrogens (c.) will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232253
An optically active compound having molecular formula $\mathrm{C}_{2} \mathrm{H}_{16}$ on ozonolysis gives acetone as one of the products. The structure of the compound is
1
2
3
4
Explanation:
In compound we know ozonolysis in the presence of $\mathrm{zn} / \mathrm{H}_{2} \mathrm{O}$ we get one compound as a ketone while in other we get other compound.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232257
The isomerisation of 1-butyne to 2- butyne can be achieved by treatment with
1 hydrochloric acid
2 ammoniacal silver nitrate
3 ammoniacal cuprous chloride
4 ethanolic potassium hydroxide
Explanation:
Isomerisation of 1-butyne to 2-butyne can be achieved by treatment with alcoholic $\mathrm{KoH}$. In the presence of alcoholic $\mathrm{KoH}$ it $\beta$-elimination. The isomerisation of 1-butyne to 2-butene can be also achieved by treatment with $\mathrm{NaNH}_{2}$ / liq. ammonia.
WB JEET-2017
GENERAL ORGANIC CHEMISTRY
232258
The conformations of n-butane, commonly known as eclipsed, gauche and anti-conformations can be interconverted by
1 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methyl group
2 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methylene group
3 rotation around $\mathrm{C} 1-\mathrm{C} 2$ linkage
4 rotation around $\mathrm{C} 2-\mathrm{C} 3$ linkage
Explanation:
The conformation of n-butane commonly known as eclipsed, gauche and anti-conformations can be achieved by rotation around $\mathrm{C}_{2}$ and $\mathrm{C}_{3}$ linkage
232251
The well known compounds, $(+)$ - lactic acid and (-)- lactic acid, have the same molecular formula, $\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}_{3}$. The correct relationship between them is
1 constitutional isomerism
2 geometrical isomerism
3 identicalness
4 optical isomerism
Explanation:
The correct relationship between (+) lactic acid and $(-)$ lactic acid is optical isomer because it has one assymmetric center is chiral center. Both are optical isomers because they rotate the plane of polarized light in opposite direction.
3 will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
4
Explanation:
, b, d) Exp:(A, B, D) : Tautomerism is exhibited by molecules containing one or more $\alpha$-hydrogens (c.) will not show tautomerism because its cyclic structure is not contain any $\alpha$-hydrogen.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232253
An optically active compound having molecular formula $\mathrm{C}_{2} \mathrm{H}_{16}$ on ozonolysis gives acetone as one of the products. The structure of the compound is
1
2
3
4
Explanation:
In compound we know ozonolysis in the presence of $\mathrm{zn} / \mathrm{H}_{2} \mathrm{O}$ we get one compound as a ketone while in other we get other compound.
WB JEET-2013
GENERAL ORGANIC CHEMISTRY
232257
The isomerisation of 1-butyne to 2- butyne can be achieved by treatment with
1 hydrochloric acid
2 ammoniacal silver nitrate
3 ammoniacal cuprous chloride
4 ethanolic potassium hydroxide
Explanation:
Isomerisation of 1-butyne to 2-butyne can be achieved by treatment with alcoholic $\mathrm{KoH}$. In the presence of alcoholic $\mathrm{KoH}$ it $\beta$-elimination. The isomerisation of 1-butyne to 2-butene can be also achieved by treatment with $\mathrm{NaNH}_{2}$ / liq. ammonia.
WB JEET-2017
GENERAL ORGANIC CHEMISTRY
232258
The conformations of n-butane, commonly known as eclipsed, gauche and anti-conformations can be interconverted by
1 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methyl group
2 rotation around $\mathrm{C}-\mathrm{H}$ bond of a methylene group
3 rotation around $\mathrm{C} 1-\mathrm{C} 2$ linkage
4 rotation around $\mathrm{C} 2-\mathrm{C} 3$ linkage
Explanation:
The conformation of n-butane commonly known as eclipsed, gauche and anti-conformations can be achieved by rotation around $\mathrm{C}_{2}$ and $\mathrm{C}_{3}$ linkage
