Answer:
To synthesize cis-2-methylcyclopentyl from methycyclopentanol, you need to replace the acetate hydroxyl group with acetate by inverting the configuration.
Explanation:
To understand the process, you need to understand the nucleophilic mechanism taking place in the process. This is the first stage of the process. Hydroxide is a poor leaving group, to it must be converted to a good leaving group. To effect the change, it is necessary to use p-toluenesuphate.
p-toluenesuphate is favored because this can be prepared by a reaction that alters none of the bonds attached to the stereogenic center.
The reaction of p-toluensulfonate with potassium acetate in acetic acid effects the conversion to give the final product: cis-2-methylcyclopentyl.
Answer:
Explanation:
S is in 3d period, so it has 3 levels
1 level has 2 electrons, 2d level 8 electrons, 3d level 6 electrons
Pairs of electrons are shared between two nonmetal atoms
hope this helps (:
<u>Answer:</u>
2400 mL
<u>Explanation:</u>
According to this equation, the stoichiometric ratio between 
and 
for the complete reaction is 1:2.
We know that the number of moles of can be calculated using the mole formula. (<em>number of moles = mass / molar mass</em>)
Moles of Calcium = 
= 1.5 mol
So the moles of = 
= 3.0 mol
<em>Volume of HCl solution = Moles of HCl/ concentration of HCl</em>
Volume of HCl solution = 
= 2400 mL
