Answer:
Ca3(PO4)2
Explanation:
Ca3(PO4)2 or calcium phosphate is insoluble in water.
<span>XY4Z2-->Square planar (Electron domain geometry: Octahedral) sp3d2
XY4Z-->Seesaw (Electron domain geometry: Trigonal bipyramidal) sp3d
XY5Z-->Square pyramidal (Electron domain geometry: Octahedral) sp3d2
XY2Z3-->Linear (Electron domain geometry: Trigonal bipyramidal) sp3d
XY2Z-->Bent (Electron domain geometry: Trigonal planar) sp2
XY3Z-->Trigonal pyramidal (Electron domain geometry: Tetrahedral) sp3
XY2Z2-->Linear (Electron domain geometry: Tetrahedral) sp3
XY3Z2-->T shaped (Electron domain geometry: Trigonal bipryamidal) sp3d
XY2-->Linear (Electron domain geometry: Linear) sp
XY3 Trigonal planar (Electron geometry: Trigonal planar) sp2
XY4-->Tetrahedral (Electron domain geometry: tetrahedral) sp3
XY5-->Trigonal bipyramidal (Electron domain geometry: Trigonal bipyramidal) sp3d
XY6-->Octahedral (Electron domain geometry: Octahedral) sp3d2</span>
Answer:
The fluoride which precipitates first is CaF₂
Explanation:
When F⁻ is added, CaF₂ and BaF₂ are produced following the ksp equation:
For CaF₂:
Ksp = 3.2x10⁻¹¹ = [Ca²⁺] [F⁻]²
<em>Where [Ca²⁺] = 0.075M * {35mL / (25mL + 35mL)} = 0.04375M</em>
3.2x10⁻¹¹ = [0.04375M] [F⁻]²
[F⁻]² = 7.31x10⁻¹⁰
[F⁻] = 2.7x10⁻⁵M
<h3>CaF₂ begins precipitation when [F⁻] = 2.7x10⁻⁵M.</h3>
For BaF₂:
Ksp = 1.5x10⁻⁶ = [Ba²⁺] [F⁻]²
<em>Where [Ba²⁺] = 0.090M * {25mL / (25mL + 35mL)} = 0.0375M</em>
1.5x10⁻⁶ = [0.0375M] [F⁻]²
[F⁻]² = 4x10⁻⁵
[F⁻] = 6.3x10⁻³M
BaF₂ begins precipitation when [F⁻] = 6.3x10⁻³M
Thus, the fluoride which precipitates first is CaF₂
Answer:
They're sexual reproduction
Explanation:
A flower throws seed at another flower
The difference of the structures of the two isomers are shown in the picture. Generally, cyclic alkanes are much easier to break than straight-chained alkanes. When the molecules are cyclic, they are close to each other, thus lesser bond angles. Because they are closer, repulsion forces could be greater than attractive forces. That is why cyclohexane needs lesser energy of 936 kcal/mol compared to 941 kcal/mol because there is an additional straight-chained methyl substituent to break in methylcyclopentane.
