is it possible to be not opticall active even though all carbons are chiral?

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yes if the compound is meso, then it wont be optically active. Meso = a line of symetry.
 
I see one question from Kaplan. This one is not meso and chiral, but it was not optically active.:scared:
 
To be more specific, a racemate is a molecule that has equal amounts of R and S. Therefore, the R will rotate polarized light lets say at an alpha bracket of 15, while S will rotate it at exactly an alpha bracket of -15, hence showing no optical activity.

racemic mixture is not optically active?

isn't racimic mixture consisted of R and S?
 
To be more specific, a racemate is a molecule that has equal amounts of R and S. Therefore, the R will rotate polarized light lets say at an alpha bracket of 15, while S will rotate it at exactly an alpha bracket of -15, hence showing no optical activity.

Yep
 
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