The answer is- is octahedral in electronic and molecular geometry with 6 Fluorine atoms bonded to central atom S.
Lewis structures are the diagrams in which the valence electrons of the atoms of a compound are arranged around the atoms showing the bonding between the atom and the lone pair of electrons existing in the molecule.
Determine the molecular geometry of .
- Valence Shell Electron Pair Repulsion theory is commonly known as VSEPR theory and it helps to predict the geometry of molecules.
- According to this theory, electrons are arranged around the central atom of the molecule in such a way that there is minimum electrostatic repulsion between these electrons.
- Now, calculate the total number of valence electrons in .
Valence electrons of S = 6
Valence electrons of F = 7
Thus, the valence electrons in are-
- The Lewis structure of is - (Image attached).
- In the structure, the number of atoms bonded to central atom (S) = 6.
- Number of non-bonding electron pairs on the central atom = 0 (as all the valence electrons are bonded to F).
- Electronic geometry in case of 6 bond pairs is octahedral.
- Molecular geometry us also octahedral with bond angles 90°.
- Central atom is sp3d2 hybridised.
- is a non-polar molecule.
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Answer:
Gibbs free energy equation
Explanation:
Answer:
The series of chemical reactions that are used to change natural resources into synthetic products is called chemical synthesis. To make a "natural" product, the natural resource is not chemically changed as much. ... For example, the synthetic material plastic is made from petroleum, which is pumped out of the earth.
Explanation:
give brainliest!!!!
Answer:
8.88 x 10⁻² M/s
Explanation:
The rate of reaction for:
NO(g) + Cl₂ (g) ⇒ 2NOCl(g)
is rate = -ΔNO/Δt = -ΔCl2/Δt = 1/2 ΔNOCl/Δt
so ΔNOCl/Δt = 2 ΔCl2/Δt = 2 x 4.44 × 10⁻² M/s = 8.88 x 10⁻² M/s
In general given a reaction
aA + bB ⇒ cC + dD
rate = -1/a ΔA/Δt = -1/b ΔB/Δt = 1/c ΔC/Δt = 1/d ΔD/Δt
Answer:
See explanation below
Explanation:
The first two pictures show the reagents used in these reactions a) and b). As it was stated, An E2 reaction proceeds with an antiperiplanar stereochemistry, so in the case of reaction a) it fill form a product with the groups in opposite directions. In other words, a Trans product.
In the case of reaction b) we have the same reaction, with the difference that we have changed the CH3 and phenyl group of positions. This will cause that the reaction will proceed the same but the stereochemistry of the final product will be changed too. In this case, and according to the picture 3 attached, we can see that the product formed is a cis product. So we can conclude that the relation of product a) and b) is that they are isomers, the trans and cis isomers respectively. See picture below for mechanism and products