This chemistry question involves key chemical concepts and calculations. The detailed solution below walks through each step, from identifying the reaction type to computing the final answer.

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Answer
C. 3-methylhex-3-ene
To determine the IUPAC name for the given compound, we follow these steps:
Step 1: Identify the longest continuous carbon chain that contains the double bond. The structure is:
CH2-CH3
|
CH3-CH2-CH=C-CH3
We can trace two possible main chains containing the double bond:
According to IUPAC rules, the longest chain containing the double bond is the parent chain. Therefore, the 6-carbon chain (hexene) is the parent chain.
Step 2: Number the carbon atoms in the parent chain such that the double bond receives the lowest possible number. The parent chain is . The methyl group is attached to one of the carbons of the double bond.
Step 3: Choose the numbering that gives the substituent the lowest possible number. Both numbering schemes give the double bond the same position (starting at C3). In such cases, we choose the numbering that gives the substituent the lowest number.
Step 4: Construct the full IUPAC name. The parent chain is a 6-carbon alkene with a double bond starting at position 3, so it's "hex-3-ene". There is a methyl group at position 3. Combining these, the name is 3-methylhex-3-ene.
Comparing this with the given options: A. 4-ethylpent-3-ene B. 2-ethylpent-2-ene C. 3-methylhex-3-ene D. 4-methylhex-3-ene
The correct option is C.
The final answer is .
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To determine the IUPAC name for the given compound, we follow these steps: Step 1: Identify the longest continuous carbon chain that contains the double bond.
This chemistry question involves key chemical concepts and calculations. The detailed solution below walks through each step, from identifying the reaction type to computing the final answer.