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

Write the isomers of the compound having the formula C4H9Br.

Advertisements
Advertisements

प्रश्न

Write the isomers of the compound having the formula C4H9Br.

दीर्घउत्तर
Advertisements

उत्तर

C4H9Br is a saturated compound because its parent hydrocarbon is C4H10.

Its isomers are as follows:

(i) \[\ce{\underset{1-Bromobutane}{CH3 - CH2 - CH2 - CH2 - Br}}\]

(ii) \[\begin{array}{cc}
\phantom{.........}\ce{Br}\\
\phantom{.......}|\\
\ce{\underset{2-Bromobutane}{CH3-CH2-CH-CH3}}
\end{array}\]

(iii) \[\begin{array}{cc}
\ce{CH3}\phantom{...}\\
|\phantom{......}\\
\ce{\underset{1-Bromo-2-Methylpropane}{CH3-CH-CH2Br}}
\end{array}\]

(iv) \[\begin{array}{cc}
\phantom{..}\ce{CH3}\\
|\phantom{..}\\
\ce{CH3 - C - Br}\phantom{.....}\\
|\phantom{..}\\
\phantom{..}\ce{\underset{2-Bromo-2-Methylpropane}{CH3}}
\end{array}\]

shaalaa.com
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 6: Haloalkanes and Haloarenes - Exercises [पृष्ठ १८९]

APPEARS IN

एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 6 Haloalkanes and Haloarenes
Exercises | Q 6.6 | पृष्ठ १८९

संबंधित प्रश्न

How do you convert the following:

Ethanol to propanenitrile


Given reasons: C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.


In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?


Arrange the compounds of the following set in order of reactivity towards SN2 displacement:

2-Bromo-2-methylbutane, 1-Bromopentane, 2-Bromopentane


C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.


What is the action of the following on ethyl bromide?

moist silver oxide


In a coordination entity of the type [PtCl2(en)2]2+ which isomer will show optical isomerism?


Which of the following is a primary halide?


Which among MeX, RCH2X, R2CHX and R3CX is most reactive towards SN2 reaction?


Which of the following is a chiral compound?


Among the following, the dissociation constant is highest for:


Identify X and Y in the following sequence:

\[\ce{C2H5Br ->[X] Product ->[Y] C3H7NH2}\]


Compound ‘A’ with molecular formula \[\ce{C4H9Br}\] is treated with aq. \[\ce{KOH}\] solution. The rate of this reaction depends upon the concentration of the compound ‘A’ only. When another optically active isomer ‘B’ of this compound was treated with aq. \[\ce{KOH}\] solution, the rate of reaction was found to be dependent on concentration of compound and \[\ce{KOH}\] both.

(i) Write down the structural formula of both compounds ‘A’ and ‘B’.

(ii) Out of these two compounds, which one will be converted to the product with inverted configuration.


Which of the following is the definition of chirality?


Which one is the correct order of nucleophilic strength (pKa) of following nucleophiles?


Give reason for the following:

The product formed during SN1 reaction is a racemic mixture.


Assertion (A) : Nucleophilic substitution of iodoethane is easier than chloroethane.

Reason (R) : Bond enthalpy of C-I bond is less than that of C-Cl bond.


Which one of the following chlorohydrocarbons readily undergoes solvolysis?


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×