Question:

The correct structure of 2,6-Dimethyl-dec-4-ene is :

Updated On: Nov 13, 2025
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The Correct Option is B

Solution and Explanation

In order to determine the correct structure of 2,6-Dimethyl-dec-4-ene, we must analyze its IUPAC name step-by-step to deduce the structure:

  1. Base Chain Identification: The base chain is "dec" which indicates that the carbon chain consists of 10 carbon atoms.
  2. Type of Bond: The suffix "-4-ene" indicates that there is a double bond located at the 4th carbon-carbon position within the chain.
  3. Substituents: The substituents are indicated by "2,6-Dimethyl." This means there are methyl groups (-CH3) attached to the 2nd and 6th carbon atoms of the main chain.

Here's the step-by-step construction of the compound:

  • Start by drawing a straight chain of 10 carbon atoms.
  • Place a double bond between the 4th and 5th carbon atoms, as the "-4-ene" indicates.
  • Attach methyl groups to the 2nd and 6th carbon atoms of the carbon chain.

Now, let's compare this structure with the given options. The correct image should reflect this arrangement: 10 carbon atoms in the main chain with the specified double bond and both methyl groups correctly positioned.

This representation correctly aligns with the requirements of the IUPAC name.

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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