Ca(OH)₂ ==> Ca²⁺ + 2 OH<span>-
Ca(OH)</span>₂ is <span>strong Bases</span><span>
</span>Therefore, the [OH-] equals 5 x 10⁻⁴ M. For every Ca(OH)₂ you produce 2 OH⁻<span>.
</span>
pOH = - log[ OH⁻]
pOH = - log [ <span>5 x 10⁻⁴ ]
pOH = 3.30
pH + pOH = 14
pH + 3.30 = 14
pH = 14 - 3.30
pH = 10.7
hope this helps!</span>
Explanation:
According to the given data, we will calculate the following.
Half life of lipase 
= 8 min x 60 s/min
= 480 s
Rate constant for first order reaction is as follows.
= 
Initial fat concentration 
= 45 
= 45 mmol/L
Rate of hydrolysis 
= 0.07 mmol/L/s
Conversion X = 0.80
Final concentration (S) = 
= 45 (1 - 0.80)
= 9
or, = 9 mmol/L
It is given that 
= 5mmol/L
Therefore, time taken will be calculated as follows.
t = ![-\frac{1}{K_{d}}ln[1 - \frac{K_{d}}{V}{K_{M} ln (\frac{S_{o}}{S}) + (S_{o} - S)]](https://tex.z-dn.net/?f=-%5Cfrac%7B1%7D%7BK_%7Bd%7D%7Dln%5B1%20-%20%5Cfrac%7BK_%7Bd%7D%7D%7BV%7D%7BK_%7BM%7D%20ln%20%28%5Cfrac%7BS_%7Bo%7D%7D%7BS%7D%29%20%2B%20%28S_%7Bo%7D%20-%20S%29%5D)
Now, putting the given values into the above formula as follows.
t =
= ![-\frac{1}{1.44 \times 10^{-3}s^{-1}}ln[1 - \frac{1.44 \times 10^{-3}s^{-1}}{0.07 mmol/L/s }{K_{M} ln (\frac{45 mmol/L }{9 mmol/L }) + (45 mmol/L - 9 mmol/L )]](https://tex.z-dn.net/?f=-%5Cfrac%7B1%7D%7B1.44%20%5Ctimes%2010%5E%7B-3%7Ds%5E%7B-1%7D%7Dln%5B1%20-%20%5Cfrac%7B1.44%20%5Ctimes%2010%5E%7B-3%7Ds%5E%7B-1%7D%7D%7B0.07%20mmol%2FL%2Fs%0A%7D%7BK_%7BM%7D%20ln%20%28%5Cfrac%7B45%20mmol%2FL%0A%7D%7B9%20mmol%2FL%0A%7D%29%20%2B%20%2845%20mmol%2FL%20-%209%20mmol%2FL%0A%29%5D)
= 
= 27.38 min
Therefore, we can conclude that time taken by the enzyme to hydrolyse 80% of the fat present is 27.38 min.
Answer:
we will except an increase in the polarity of the system and this will cause the Non-polar spot to be near the solvent front, while the polar spot will run at an approximate speed of 0.5 Rf
Explanation:
when we run a TLC plate in a 50/50 mixture of hexanes and ethyl acetate we will except an increase in the polarity of the system and this will cause the Non-polar spot to be near the solvent front, while the polar spot will run at an approximate speed of 0.5 Rf
The speed of the polar spot depends largely on the level of polarity, an increase in the polarity will see both spots of Neat hexane run when we run a TLC plate in a 50/50 mixture of hexanes and ethyl acetate
Well assuming we have all of these, earth
Answer:
Axial
Explanation:
In the most stable conformation of Cis-3-tert-Butylcyclohexanol, the tert-butyl group is at equatorial position and the alcohol group is in the axial position.
If the tert-butyl group is placed in equatorial position, repulsions are minimized. The bulkier the group, the greater the energy difference between the axial and equatorial conformers. Hence for a ring having a bulky substituent, such bulky substituent is better placed in the equatorial position.
The energy difference between the conformers of Cis-3-tert-Butylcyclohexanol is so high that the compound is almost "frozen" in a conformation where the tert-butyl groups are equatorial and the -OH groups are axial. This conformer is more stable by 24 KJ/mol.
