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2 years ago

Summarize how a dinosaur can become a fossil.

1 answer:

3 0

The dinosaur dies and is washed away in a flood. The body is buried in sediment (mud or sand) and eventually the body is covered. ... Eventually, the fossil skeleton comes to the surface and is discovered.

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Water has a boiling point of 100.0°C and a Kb of 0.512°C/m. What is the boiling

Reil [10]

Answer:

The boiling point of a 8.5 m solution of Mg3(PO4)2 in water is 394.91 K.

Explanation:

The formula for molal boiling Point elevation is :

$\Delta T_{b} = iK_{b}m$

$\Delta T_{b}$ = elevation in boiling Point

$K_{b}$ = Boiling point constant( ebullioscopic constant)

m = molality of the solution

i = Van't Hoff Factor

Van't Hoff Factor = It takes into accounts,The abnormal values of Temperature change due to association and dissociation .

In solution Mg3(PO4)2 dissociates as follow :

$Mg_{3}(PO_{4})_{2}\rightarrow 3Mg^{2+} + 2 PO_{4}^{3-}$

Total ions after dissociation in solution :

= 3 ions of Mg + 2 ions of phosphate

Total ions = 5

i = Van't Hoff Factor = 5

m = 8.5 m

$K_{b}$ = 0.512 °C/m

Insert the values and calculate temperature change:

$\Delta T_{b} = iK_{b}m$

$\Delta T_{b} = 5\times 0.512\times 8.5$

$\Delta T_{b} = 21.76 K$

Boiling point of pure water = 100°C = 273.15 +100 = 373.15 K

$\Delta T_{b} = T_{b} - T_{b}_{pure}$

$T_{b}_{pure}$ = 373.15 K[/tex]

21.76 = T - 373.15

T = 373.15 + 21.76

T =394.91 K

8 0

3 years ago

Complete the mechanism for the base-catalyzed opening of the epoxide below by adding any missing atoms, bonds, charges, nonbondi

worty [1.4K]

Complete Question:

check the first image for complete part of the question

Answer and Explanation:

Epoxide is a three membered ring made up of two carbon atoms and one oxygen atom. Epoxides are cyclic ethers. Due to its ring size, it is highly strained and very reactive. Epoxide ring opening takes place with respect to addition of acid and base.

Ring opening of epoxide with acid:

In the presence of base, the nucleophile attacks the epoxide ring at more substituted site and inverse stereochemistry takes place.(check file 2 attached)

Ring opening of epoxide with base:

The backside attack of nucleophile takes place in less substituted site and then it undergoes protonation to form a product.

(check file 2 attached)