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For 1-methoxy-1,3-butadiene, which of the following resonating structure is the least stable ? [JEE-2005]
- a)
- b)
- c)
- d)
Correct answer is option 'C'. Can you explain this answer?
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Verified Answer
For 1-methoxy-1,3-butadiene, which of the following resonating structu...
There is no conjugation stability, two double bonds are together and -ve charge & lone pair (on oxygen) are also together in option C
Also carbon having + charge form more than 4 bonds, thus breaking the rule of tetra-valancy.
Hence C
Most Upvoted Answer
For 1-methoxy-1,3-butadiene, which of the following resonating structu...
Because in (c) part there is no conjugation stability [such as two double bonds are together & -ve charge & lone pair (on oxygen) are also together in (c) option]
& also carbon having + charge form more than 4 bonds (break there rule of tetravalency)..
& also carbon having + charge form more than 4 bonds (break there rule of tetravalency)..
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Community Answer
For 1-methoxy-1,3-butadiene, which of the following resonating structu...
There is no conjugation stability, two double bonds are together and -ve charge & lone pair (on oxygen) are also together in option C
Also carbon having + charge form more than 4 bonds, thus breaking the rule of tetra-valancy.
Hence C
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For 1-methoxy-1,3-butadiene, which of the following resonating structure is the least stable ? [JEE-2005]a)b)c)d)Correct answer is option 'C'. Can you explain this answer?
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