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Due to angle strain , the three membered ring is not stable. So i think it would break and kick out one of the chlorine atoms resulting in the formation of a carbene. But i don't know how to proceed further and how it finally breaks into 2 products.

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As I mentioned in the comments, this is a simple homolytic bond fission to give a carbene and a stable aromatic compound (Phenanthrene). Here's the mechanism: enter image description here

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