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

(i) Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names. (ii) Classify the isomers of alcohols in the above question as primary, secondary and tertiary - Chemistry

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प्रश्न

  1. Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names.
  2. Classify the isomers of alcohols in the above question as primary, secondary and tertiary alcohols.
रासायनिक समीकरण/संरचनाएँ
अति संक्षिप्त उत्तर
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उत्तर

i. The isomeric alcohols with molecular formula C5H12O are –

(a) \[\ce{\underset{Pentanol (1^\circ)}{CH3 - CH2 - CH2 - CH2 - CH2 - OH}}\]

 

(b) \[\begin{array}{cc}
\ce{CH3 - CH2 - CH2 - \overset{∗}{C}H - CH3}\\
\phantom{............}|\\
\phantom{...............}\ce{\underset{Pentan-2-ol (2^\circ)}{OH}}\
\end{array}\]

 

(c) \[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH2 - CH3}\\
|\phantom{..}\\
\phantom{..}\ce{\underset{Pentan-3-ol (2^\circ)}{OH}}\
\end{array}\]

 

(d) \[\begin{array}{cc}
\ce{H3C - H2C - H\overset{∗}{C} - CH2OH}\\
\phantom{.....}|\\
\phantom{.........}\ce{\underset{2-Methylbutan-1-ol (1^\circ)}{CH3}}\
\end{array}\]

 

(e) \[\begin{array}{cc}
\ce{CH3}\phantom{............}\\
|\phantom{...............}\\
\ce{\underset{3-Methylbutan-1-ol (1^\circ)}{CH3 - CH - CH2 - CH2 - OH}}\\
\end{array}\]

 

(f) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3 - C - CH2 - CH3}\\
|\phantom{.......}\\
\ce{\underset{2-Methylbutan-2-ol (3^\circ)}{OH}}\phantom{....}\
\end{array}\]

 

(g) \[\begin{array}{cc}
\ce{CH3}\phantom{...}\\
|\phantom{......}\\
\ce{CH3 - C - CH2 - OH}\\
|\phantom{......}\\
\ce{\underset{2, 2-Dimethylpropan-1-ol (1^\circ)}{CH3}}\phantom{..}\
\end{array}\]

 

(h) \[\begin{array}{cc}
\phantom{.}\ce{CH3}\phantom{...}\ce{OH}\\
|\phantom{......}|\phantom{..}\\
\ce{\underset{3-Methylbutan-2-ol (2^\circ)}{CH3 - CH - \underset{∗}{C}H - CH3}}\
\end{array}\]

Isomers (b), (d) and (h) contain chiral carbon atoms; thus, they exhibit enantiomerism.

ii. Isomers (a), (d), (e) and (g) are primary alcohols.

Isomers (b), (c) and (h) are secondary alcohols.

Isomer (f) is a tertiary alcohol.

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अध्याय 7: Alcohols, Phenols and Ethers - Exercises [पृष्ठ २२२]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 7 Alcohols, Phenols and Ethers
Exercises | Q 7.3 | पृष्ठ २२२

संबंधित प्रश्न

Write IUPAC name of the following compound:

C6H5 – O – C7H15(n−)


What is the action of hot HI on it?


How is phenol converted into the following?

Benzene


Write structural formula for Methyl vinyl ether.


An example of a compound with functional group – O – is ____________.


Ethylene reacts with Baeyer’s reagent to give ______.


Match the starting materials given in Column I with the products formed by these (Column II) in the reaction with HI.

  Column I   Column II
(i) CH3—O—CH3 (a)
(ii) \[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
\backslash\phantom{.............}\\
\ce{CH-O-CH3}\\
/\phantom{..............}\\
\ce{CH3}\phantom{..................}
\end{array}\]
(b) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-I + CH3OH}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]
(iii) \[\begin{array}{cc}
\ce{CH3}\phantom{.}\\
|\phantom{....}\\
\ce{H3C-C-O-CH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]
(c)
(iv) (d) CH3—OH + CH3—I
    (e) \[\begin{array}{cc}
\ce{CH3}\phantom{.....................}\\
\backslash\phantom{.................}\\
\ce{CH-OH + CH3I}\\
/\phantom{.................}\\
\ce{CH3}\phantom{.....................}
\end{array}\]
    (f) \[\begin{array}{cc}
\ce{CH3}\phantom{.....................}\\
\backslash\phantom{.................}\\
\ce{CH-I + CH3OH}\\
/\phantom{.................}\\
\ce{CH3}\phantom{.....................}
\end{array}\]
    (g) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-OH + CH3I}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]

Assertion: p-nitrophenol is more acidic than phenol.

Reason: Nitro group helps in the stabilisation of the phenoxide ion by dispersal of negative charge due to resonance.


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Reason: –OH group in phenol is o–, p– directing.


Write the IUPAC name of the following compound.


Write a chemical reaction for the following conversion:

Acetic acid into ethyl alcohol.


How are the following conversions carried out?

Methyl magnesium bromide→2-Methylpropan-2-ol.


Draw structure of the following compound.

2-Methoxypropane


Draw structure of the following compound.

Prop-2-en-1-ol


Write structural formulae for:

p-Nitrophenol


Write structural formulae for:

Salicylic acid


The IUPAC name of is ______.


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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