मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Write structure of the compound whose IUPAC names is 3-Chloromethylpentan-1-ol

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प्रश्न

Write structures of the compounds whose IUPAC names are as follows:

3-Chloromethylpentan-1-ol.

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उत्तर

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संबंधित प्रश्‍न

Write IUPAC name of the following compound:


Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.

(A) formaldehyde

(B) acetaldehyde

(C) acetone

(D) ethyl methyl ketone


Which of the following compounds is NOT prepared by the action of alcoholic NI3 on alkyl halide?

(a) CH3NH2

(b) CH3- CH2- NH2

(c) CH3 - CH2 - CH2 - NH2

(d) (CH3)C- NH2


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How is phenol converted into the following?

benzoquinone


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(1) formation of carbonation

(2) formation of an ester

(3) protonation of the alcohol molecule

(4) elimination of water


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Write structural formula for pentane-1,4-diol.


C6H5OCH2CH3 is called:


The compound HOCH2 – CH2OH is __________.


n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent?


The product of acid catalysed hydration of 2-phenylpropene is:


\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]

The product ‘Z’ is:


IUPAC name of the compound is:

\[\begin{array}{cc}
\ce{CH3-CH-OCH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]


IUPAC name of the compound \[\begin{array}{cc}
\ce{CH3 - CH - OCH3}\\
\phantom{}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{..}
\end{array}\] is ______.


Write the IUPAC name of the compound given below.

\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH2 - C = C - OH}\\
\phantom{........}|\phantom{....}|\phantom{}\\
\phantom{..............}\ce{CH3 CH2OH}
\end{array}\]


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Reason: Bromine polarises in carbon disulphide.


Write a chemical reaction for the following conversion:

Acetic acid into ethyl alcohol.


Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.


Write the IUPAC name of the following compound:

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


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