Question:

The compound that will react most readily with gaseous bromine has the formula

Updated On: Apr 20, 2025
  • ${ C3H6}$
  • ${ C2H2 }$
  • ${C4H_{10 } }$
  • ${ C2H4}$
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The Correct Option is A

Solution and Explanation

Reactivity of Propene towards Bromine 

Propene is more reactive towards \(\text{Br}_2\) (gaseous) than \(\text{CH}_2=\text{CH}_2\) (ethylene), \(\text{HC} = \text{CH}\) (acetylene), and butane. This is due to the greater electron density in propene.

Explanation:

In the case of alkene reactions with bromine, the reactivity depends on the availability of electron density for the electrophilic addition reaction. In the case of propene:

  • Propene: The double bond in propene has more electron density due to the alkyl group (–CH₃) attached to the carbon of the double bond, making it more nucleophilic and more reactive towards electrophilic reagents like \(\text{Br}_2\).
  • Ethylene (CH₂=CH₂): Ethylene has less electron density than propene as there are no alkyl groups donating electron density to the double bond.
  • Acetylene (HC≡CH): Acetylene has a triple bond, which is electron-deficient compared to the double bond in propene, making it less reactive towards bromine.
  • Butane: Butane is a saturated hydrocarbon, meaning there is no double bond available for electrophilic attack, and thus it doesn't react with bromine in the same way as the alkenes do.

Conclusion:

Propene is the most reactive towards gaseous bromine because the electron density around the double bond is higher compared to the other molecules, facilitating a faster electrophilic addition reaction.

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Concepts Used:

Alkenes

Alkenes

In organic chemistry, an alkene is a hydrocarbon containing a carbon-carbon double bond.[1]

Alkene is often used as synonym of olefin, that is, any hydrocarbon containing one or more double bonds.

Read More: Ozonolysis

IUPAC Nomenclature of Alkenes

  1. An alkene or cycloalkene is indicated by the suffix (ending) ene.
  2. For the root name, the longest chain must include both carbon atoms of the double bond.
  3. The root chain must be numbered beginning at the end closest to a double bond carbon atom. If the double bond is in the chain's centre, the nearest substituent rule is used to determine where the numbering begins.
  4. If the compound contains more than one double bond, it is named with a diene, triene, or equivalent prefix indicating the number of double bonds, and each double bond is assigned a locator number.

Read More: Unsaturated Hydrocarbon