HSC Science (Electronics) ११ वीं कक्षा - Maharashtra State Board Question Bank Solutions

Name the types of intermolecular forces present in Cl₂.

Name the types of intermolecular forces present in CCl₄.

Name the types of intermolecular forces present in HNO₃.

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\ce{H} \phantom{...}\ce{H}\\
|\phantom{....}|\\
\ce{N ≡ C - C - C - C ≡ N}\\
|\phantom{....}|\\
\ce{H} \phantom{...}\ce{H}
\end{array}\]

Write dash formulae for the following bond line formulae.

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\ce{H}\phantom{...}\ce{H}\\
|\ \phantom{....} |\\
\ce{N ≡ C - C - C - C ≡ N}\\
|\ \phantom{....} |\\
\ce{H}\phantom{....}\ce{H}
\end{array}\]

Write dash formulae for the following bond line formulae.

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\ce{H} \phantom{...}\ce{H}\phantom{...} \ce{H} \phantom{...}\ce{H}\\
|\phantom{....}|\phantom{....}|\phantom{....}|\\
\ce{H - C - C - C - C - H}\\
|\phantom{....}|\phantom{....}|\phantom{....}|\\
\ce{H}\phantom{...} \ce{H}\phantom{...} \ce{H}\phantom{...} \ce{H}
\end{array}\]

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\
|\ \phantom{....} |\ \phantom{....} |\ \phantom{....} |\\
\ce{H - C - C - C - C - H}\\
|\ \phantom{....} |\ \phantom{....} |\ \phantom{....} |\\
\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}
\end{array}\]

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\phantom{......}\ce{H}\phantom{...} \ce{H} \phantom{...}\ce{H}\phantom{....} \ce{O}\\
\phantom{......}|\phantom{....}|\phantom{....}|\phantom{....}// \\
\ce{H - C - C - C - C }\\
\phantom{......}|\phantom{....}|\phantom{....}|\phantom{.....}\backslash \\
\phantom{..........}\ce{H}\phantom{...} \ce{H} \phantom{...}\ce{H}\phantom{....} \ce{OH}\phantom{...}
\end{array}\]

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\ce{H}\phantom{....}\ce{H}\phantom{....}\ce{H}\phantom{...}\ce{O}\phantom{......}\\
|\ \phantom{....}|\ \phantom{....}|\ \phantom{...} //\phantom{...}\phantom{...}\\
\ce{H - C - C - C - C}\phantom{...........}\\
|\ \phantom{....}|\ \phantom{....}|\ \phantom{...}\backslash\phantom{......}\\
\ce{H}\phantom{...}\ce{H}\phantom{....} \ce{H}\phantom{....} \ce{OH}\phantom{...}
\end{array}\]

Write bond line formulae and condensed formulae for the following compound.

2, 2, 4, 4- tetramethylpentane

Write the structural formulae for the following name and also write correct IUPAC name for them.

2,2,3-trimethylpentan-4-ol

Write bond line formulae and condensed formulae for the following compound.

2, 2, 4, 4- tetramethylpentane

Write the structural formulae for the following names and also write correct IUPAC names for them.

2,2,3-trimethylpentan-4-ol

Acetone and acetaldehyde are the ozonolysis products of an alkene. Write the structural formula of an alkene and give the IUPAC name of it.

Read the following reaction and answer the questions given below.

\[\begin{array}{cc}
\ce{CH3 - C = CH2 + HBr ->[benzoyl][peroxide] CH3}\\
\phantom{.....}|\phantom{........................}|\phantom{}\\
\phantom{.................}\ce{CH3}\phantom{..............}\ce{CH3 - CH\ - CH2Br}\phantom{}\
\end{array}\]

a. Write the IUPAC name of the product.

b. State the rule that governs the formation of this product.

Write the condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{}\\
\phantom{}|\phantom{....}|\phantom{}\\
\ce{N ≡ C - C - C - C ≡ N}\\
\phantom{}|\phantom{....}|\phantom{}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{}\\
\end{array}\]

Write dash formulae for the following bond line formulae.

Write condensed formulae and bond line formulae for the following structure.

\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{}\\
\ce{H - C - C - C - C - H}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{}\\
\end{array}\]