हिंदी

For the isomeric dihalobenzenes, melting point of __________ - Chemistry

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प्रश्न

For the isomeric dihalobenzenes, melting point of __________

विकल्प

  • ortho isomer is higher

  • meta isomer is higher

  • para isomer is higher

  • all isomers is nearly same

MCQ
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उत्तर

For the isomeric dihalobenzenes, melting point of para isomer is higher

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Optical Isomerism in Halogen Derivatives
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 10: Halogen Derivatives - Multiple choice questions

APPEARS IN

एससीईआरटी महाराष्ट्र Chemistry [English] 12 Standard HSC
अध्याय 10 Halogen Derivatives
Multiple choice questions | Q 3

संबंधित प्रश्न

Identify the chiral molecule from the following.


Explain optical isomerism in 2-chlorobutane.


Optical activity of a molecule is associated with _______________


Explain optical activity of 2-chlorobutane.


Which among the following compounds in crystalline form is used for making Nicol's prism?


Which of the following is NOT a chiral molecule?


The number of optical isomers possible for 3, 4-dichloropentan-2-ol is ______.


Calcite crystals used in Nicol's prism are formed of ______.


(+) 2-methylbutan-1-ol (-) 2-methylbutan- 1-ol have different values for which property?


Identify the chiral molecule from the following.


Identify the chiral molecule from the following.


Identify the chiral molecule from the following.


Identify chiral molecules from the following

a.

\[\begin{array}{cc}
\ce{CH3 - CH - CH2 - CH3}\\
|\phantom{.........}\\
\ce{OH}\phantom{.......}
\end{array}\]

b.

\[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH2 - CH3}\\
|\phantom{..}\\
\ce{Br}
\end{array}\]

c.

\[\begin{array}{cc}
\ce{CH3 - CH2 - CH2 - CH2Br}
\end{array}\]

d.

\[\begin{array}{cc}
\ce{CH3 - CH - CH3 - CH3}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]


What is dextrorotatory substance?


Identify the chiral molecule from the following.


Identify chiral molecules from the following.

a.

\[\begin{array}{cc}
\ce{CH3 - CH - CH2 - CH3}\\
|\phantom{.........}\\
\ce{OH}\phantom{.......}
\end{array}\]

b.

\[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH2 - CH3}\\
|\phantom{..}\\
\ce{Br}\phantom{.}
\end{array}\]

c.

\[\begin{array}{cc}
\ce{CH3 - CH2 - CH2 - CH2 - Br}
\end{array}\]

d.

\[\begin{array}{cc}
\ce{CH3 - CH - CH3 - CH3}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]


Identify the chiral molecule from the following.


Identify chiral molecule/s from the following.


Identify chiral molecule/s from the following.


Identify the chiral molecule from the following.


Identify the chiral molecule from the following.


Identify chiral molecule/s from the following.


Identify the chiral molecule from the following.


Identify chiral molecule/s from the following.


Identify chiral molecule/s from the following.


Identify the chiral molecule from the following.


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