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###### Question 3 Not yet answered Marked out of 3.00 P Flag question How can chloride attack...

Question 3 Not yet answered Marked out of 3.00 P Flag question How can chloride attack the positively charged carbocation (left), which is surrounded by sterically bulky methyl and ethyl groups? 10 + CH fast Select one or more: O a. The carbocation is now pyramidal, so the carbon is open to attack o b. The elactrostatic attraction between the positively-charged carbon and negatively charged chloride overcome steric considerations c. The positive charge on the carbon pushes the methyl and ethyl groups further away, so the carbon is open for attack O d. The carbocation is roughly planar, so the carbon is open to attack

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