Draw the structure of the bromohydrin formed when (E)-2-hexene reacts with Br, H20. Use the wedge hash bond tools to indicate stereochemistry where it exists.

• If the reaction produces a racemic mixture, draw both stereoisomers.

Separate multiple products using the - sign from the drop-down menu.

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See explanation and image attached

Explanation:

The addition of a halohydrin to an alkene proceeds via the bromium cyclic intermediate.

The bromine dissociates heterolytically and attacks the (E)-2-hexene yielding the brominuim ion intermediate. This is now attacked by water with a consequent loss of H^+ to yield the final product.

Since the reaction involves a flat and planar carbocation intermediate, racemization is possible, thereby leading to the two stereoisomers shown in the image attached to this answer.

the density(ratio between mass and volume as m/v) decreases from top to bottom in periodic table group as the size increases and nuclear charge decreases. but in periods density increases from left to right as atom size decreases and nuclear charge increases.

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