<h3>Answer:</h3>
The three possible stereoisomers of 1,3-cyclopentanediol are as follow,
i) (1S,3R)-1,3-Cyclopentanediol
ii) (1R,3R)-1,3-Cyclopentanediol
iii) (1S,3S)-1,3-Cyclopentanediol
Structures of all three compounds are attached below.
<h3>Explanation:</h3>
Stereoisomers: Also known as spatial isomers are those isomers which have same molecular formula and structural formula but the groups about the chiral center occupy different orientation in space.
Enantiomers: These are stereoisomers of each other which are non-identical mirror-images of each other.
Diastereomers: These are stereoisomers which are not mirror images of each other.
Meso Compounds: These are those isomers which are superimposible on its mirror image.
Answer:
<u>89.6 L</u>
Explanation:
In normal conditions,
<u><em>For every </em></u><u><em>1 mole</em></u><u><em> of carbon dioxide at STP, it occupies </em></u><u><em>22.4 L</em></u><u><em> of volume.</em></u>
<u><em /></u>
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Solving :
⇒ 1 mole : 22.4 L
⇒ 1 × 4 : 22.4 × 4
⇒ 4 moles : <u>89.6 L</u>
A solution is acidic if it’s pH is below 7