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REY [17]
3 years ago
8

In the malate aspartate shuttle, glutamate is converted to _________ in the mitochondria while aspartate is converted to _______

____ in the cytosol.
Chemistry
1 answer:
olya-2409 [2.1K]3 years ago
5 0

Answer:

α-ketoglutarate; oxaloacetate

Explanation:

In the malate aspartate shuttle, glutamate is converted to α-ketoglutarate in the mitochondria by the enzyme glutamate dehydrogenase while aspartate is converted to oxaloacetate in the cytosol by the enzyme aspartate aminotransferase.

An important enzyme in the malate aspartate shuttle, is malate dehydrogenase. In the shuttle system, it is present in the mitochondria and in the cytosol and catalyzes the enzymatic reaction in opposite direction.

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Equilibrium describes the balance that results from a forward and reverse reaction proceeding at equal rates. Since reaction rat
Delvig [45]

Answer:

b) the reaction proceeds to a new equilibrium in the direction that offsets the change.

Explanation:

According to Le Chatelier's principle, when a system experiences a constraint such as a change in pressure, temperature or concentration, the system will readjust itself in order to annul the constraint.

This simply means that when temperature, concentration or pressure is changed, a new equilibrium position is reached in order to offset the changes in the system.

5 0
3 years ago
Why is the anatomy of the human body not a general reason to study chemistry. Need help for a good reply.
ivolga24 [154]
Anatomy's a biology topic!
8 0
3 years ago
How do you solve this ?NH4+NO4->N2+O2+H2O2
ololo11 [35]
I'm assuming you wanted this equation balanced? If you typed it correctly, it's already balanced for you. :)
8 0
3 years ago
Morphine has the formula c17h19no3. it is a base and accepts one proton per molecule. it is isolated from opium. a 0.685 −g samp
kotykmax [81]
2 C₁₇H₁₉NO₃ + H₂SO₄ → Product
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percent morphine = \frac{mass of morphine}{mass of opium} x 100
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7 0
3 years ago
Name a possible product of this reaction in the presence of ether and AlCl3: methylbenzene + 1-chlorodecane.a. 1-methyl-2-decylb
Vikki [24]

Answer:

None of these

Explanation:

Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.

Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :

Step -1 : Generation of stable carbocation.

Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.

Step-2: Attack of the ring to the carbocation

The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.

The product formed is shown in mechanism does not mention in any of the options.

So, None of these is the answer

8 0
3 years ago
Read 2 more answers
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