Answer: 37.5grams of Cu(NO3)2
Cu(1mol) + 2HNO3(2mol) —> Cu(NO3)2 + H2
<em>125 grams of Cu(1mol) reacts with 75 grams of HNO3(2mol)</em>
<em><u>HNO3 is the limiting substance, therefore, 75 grams is the limiting quantity.</u></em>
<em>Therefore, 2mol of HNO3 forms 1mol of Cu(NO3)2</em>
<em>75 grams of HNO3 forms...75grams x 1mol/2mol = 37.5 grams of Cu(NO3)2</em>
Answer:
Atoms form chemical bonds to achieve a full outer energy level, which is the most stable arrangement of electrons. A chemical bond is a force of attraction between atoms or ions
Explanation:
Explanation:
Haemoglobin consists of heme unit which is comprised of an <u>
</u> and porphyrin ring. The ring has four pyrrole molecules which are linked to the iron ion. In oxyhaemoglobin, the iron has coordinates with four nitrogen atoms and one to the F8 histidine residue and the sixth one to the oxygen. In deoxyhaemoglobin, the ion is displaced out of the ring by 0.4 Å.
The prosthetic group of hemoglobin and myoglobin is - <u>Heme</u>
The organic ring component of heme is - <u>Porphyrin</u>
Under normal conditions, the central atom of heme is - <u></u>
In <u>deoxyhemoglobin</u> , the central iron atom is displaced 0.4 Å out of the plane of the porphyrin ring system.
The central atom has <u>six</u> bonds: <u>four</u> to nitrogen atoms in the porphyrin, one to a <u>histidine</u> residue, and one to oxygen.
To completely convert 9. 0 moles of hydrogen gas (h2) to ammonia gas, 3.0 moles of nitrogen gas (n2) are required.
<h3>What are moles?</h3>
The mole is a SI unit of measurement that is used to calculate the quantity of any substance.
<h3 />
The given reaction is 
By the stoichiometry rule of ratio hydrogen: nitrogen
3 : 1
The reacted moles of nitrogen is equals to H/3 moles of reacted hydrogen
So, moles of nitrogen
Thus, 3.0 moles of nitrogen gas (n2) are required.
Learn more about moles
brainly.com/question/26416088
#SPJ4
Spectrophotometric cell or a cuvette is made of quartz for UV spectrophotometers. These cuvettes are used as sample holders for the spectrophotometric determination of the analytes. The material that makes up the cuvette and the condition of the cuvette is to be taken care of in order to avoid erroneous absorbance readings. The sample holder or the cuvette must be removed from the spectrophotometer in between two successive readings. This is to ensure that the light sensing detector of the instrument is not affected.
