The volume of the rock is 150
Answer:
The correct answer is 1 glycogen degradation would slow down.
Explanation:
Glycogen is the principle storage polysaccharide present in the liver and muscle of human body.
Glycogen contain both alpha-1,4-glycosidic linkage and alpha -1,6-glycosidic linkage.During glycogenolysis some glucose residues are transferred from branch point of the glycogen to its end and thereafter a single glucose residue is linked to the branch point of glycogen by alpha-1,6-glycosidic linkage.
The alpha-1,6-glycosidic linked glucose of glycogen is finally get separated from glycogen by the catalytic activity of alpha-1,6-glycosidase enzyme in the final step of glycogenolysis.
According to the given question if there is no alpha-1,6-glycosidic linkage in the glycogen then glycogen degradation will slow down.
Answer:
Marine life is least affected by the temperature fluctuations of the atmosphere.
Explanation:
The high specific heat capacity of water means that it takes much more energy to raise the temperatures of water by one (1) degree than land. This means that on a hot sunny day, land temperatures would increase dramatically while ocean temperatures would only rise slightly. Conversely, at night, the land cools rapidly while oceans cool slowly hence the temperatures drop slightly.
Answer: 2.8 moles
Explanation:
The balanced equation below shows that 1 mole of sodium oxide reacts with 1 mole of water to form 2 moles of sodium hydroxide respectively.
Na2O + H2O --> 2NaOH
1 mole of H2O = 2 moles of NaOH
Let Z moles of H2O = 5.6 mole of NaOH
To get the value of Z, cross multiply
5.6 moles x 1 mole= Z x 2 moles
5.6 = 2Z
Divide both sides by 2
5.6/2 = 2Z/2
2.8 = Z
Thus, 2.8moles of H2O are needed to produce 5.6 mol of NaOH
Answer:
See Explanation
Explanation:
In electrophilic aromatic substitution, the benzene ring undergoes substitution when it is reacted with suitable electrophiles.
The products of electrophilic aromatic substitution depends on the substituents already present on the benzene ring. Some substituents activate the ring towards electrophilic substitution and direct the incoming electrophile to the ortho and para positions on the ring while some substituents deactivate the benzene ring towards electrophilic substitution and direct the incoming electrophlle to the meta position on the ring.
The amide substituent is moderately activating and is an ortho, para director hence the products shown in the mage attached to this answer.
