Answer:
600 g K₂SO₄
Explanation:
First write down the complete, balanced chemical equation for such question. In this case:
Cr₂(SO₄)₃ + 2K₃PO₄ → 3K₂SO₄ + 2CrPO₄
Next, calculate molar masses of required compounds mentioned in the question. In this case it is for Cr₂(SO₄)₃ and K₂SO₄.
= 2*(MM of Cr) + 3*( MM of S) + 3*4*( MM of O)
= 2*(52) + 3*(32) + 12*(16)
= 104 + 96 + 192
= 392 g
= 2*(MM of K) + 1*( MM of S) + 4*( MM of O)
= 2*(39) + 32 + 4*(16)
= 78 + 32 + 64
= 174 g
Here comes the concept of Limiting reagent:
The limiting reagent in a chemical reaction is the substance that is totally consumed when the chemical reaction is complete. The amount of product formed is limited by this reagent, since the reaction cannot continue without it. The other reactants present with this are usually in excess and called excess reactants. If quantities of both the reactants are given, then one should apply unitary method and find out the limiting reagent out of the two. Then, determine the amount of product formed or percentage yield.
Also, 1 mole( 392 g) of Cr₂(SO₄)₃ gives 3 moles( 174*3 = 522 g) of K₂SO₄.
Using unitary method, if 392g of Cr₂(SO₄)₃ gives 522 g of K₂SO₄ , then 450 g of Cr₂(SO₄)₃ will give how much of K₂SO₄?
Yeild of K₂SO₄ :
That is 599.3 g.
Since we have not considered molecular masses of individual atoms to 6 decimal places, this number can be approximated to 600g.
Therefore, 600g of K₂SO₄ is produced.
Answer:
Two non bonded electron pairs and four bonded electron pairs
Explanation:
An image of the compound as obtained from chemlibretext is attached to this answer.
The ion ICl4- ion, is an AX4E2 ion. This implies that there are four bond pairs and two lone pairs of electrons. As expected, the shape of the ion is square planar since the lone pairs are found above and below the plane of the square. This is clear from the image attached.
Answer:
four (4)
Explanation:
Naphthalein is an organic compound with formula C 10H 8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings. It is best known as the main ingredient of traditional mothballs.
The molecule is planar, like benzene. Unlike benzene, the carbon–carbon bonds in naphthalene are not of the same length. The bonds C1−C2, C3−C4, C5−C6 and C7−C8 are about 1.37 Å (137 pm) in length, whereas the other carbon–carbon bonds are about 1.42 Å (142 pm) long. This difference, established by X-ray diffraction is consistent with the valence bond model in naphthalene and in particular, with the theorem of cross-conjugation. This theorem would describe naphthalene as an aromatic benzene unit bonded to a diene but not extensively conjugated to it (at least in the ground state), which is consistent with two of its three resonance structures.
Because of this resonance, the molecule has bilateral symmetry across the plane of the shared carbon pair, as well as across the plane that bisects bonds C2-C3 and C6-C7, and across the plane of the carbon atoms. Thus there are two sets of equivalent hydrogen atoms: the alpha positions, numbered 1, 4, 5, and 8, and the beta positions, 2, 3, 6, and 7. Two isomers are then possible for mono-substituted naphthalenes, corresponding to substitution at an alpha or beta position. Bicyclo[6.2.0]decapentaene is a structural isomer with a fused 4–8 ring system.
Therefore four (4) double bonds will be added to give each carbon atom an octet structure.
