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Bond [772]
3 years ago
14

Calcium salts give bone its a. tensile strength. b. torsional strength. c. flexibility. d. compressional strength.

Chemistry
1 answer:
makvit [3.9K]3 years ago
7 0

Answer:

Calcium salts give bone its a. tensile strength. b. torsional strength. c. flexibility. d. compressional strength.

The answer is Option D (Compressional strength)

Explanation:

Calcium is the most abundant mineral in the body, most of the calcium in the body are found in the bones and teeth. Calcium helps the body with not only building strong bones and teeth, but also assisting the body in sending and receiving nerve signals. If blood calcium gets too high or too low, the muscles and nerves will not function.

Bone which serves as a storage area for calcium are mostly made of the protein collagen, forms the skeletal framework of all vertebrates, and it plays a major role in calcium balance in the blood. Bone exhibits four types of cells: osteoblasts, bone lining cells, osteocytes, and osteoclasts. Functions of bone includes structural support of the body, protection of internal organs, attachment of the muscles, production of blood cells.

Calcium salts form crystals that give bones great strength. Bone mineral is formed from carbonated hydroxyapatite. Calcium hydroxyapatite is a naturally occurring mineral form of calcium apatite, it contains magnesium and carbonate and it is identical to the substance in teeth and bones. The collagen fibers give bone its tensile strength, and hydroxyapatite give bone its compressive strength.

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2 years ago
magine that an uncharged pith ball is brought into the electrostatic field of a charged rod. The side of the pith ball closest t
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Explanation:


This phenomenon is called electrostatic induction.


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3 years ago
2C3H7OH + 9O2 --&gt; 6CO2 + 8H2O
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Treatment of 2,4,6-tri-tert-butylphenol with bromine in cold acetic acid gives the compound C18H29BrO in quantitative yield. The
Cloud [144]

Answer:

2,4,6-tri-tert-butylcyclohexa-2,5-dienone

Explanation:

1. Information from the formulas

C₁₈H₃₀O ⟶ C₁₈H₂₉BrO

A Br has replaced an H.

2. Information from the reaction

These look like the conditions for an electrophilic aromatic substitution.

3. Possible mechanism (Fig. 1)

The product must be highly symmetrical, because there are so few NMR signals.

(i) The bromonium ion attacks at the para position, forming a resonance-stabilized carbocation intermediate.

(ii) A bromide ion attacks the H of the hydroxyl group to form 2,4,6-tri-tert-butylcyclohexa-2,5-dienone.

4. Confirmatory evidence (Fig. 2)

(a) Infrared  

1630 cm⁻¹:  C=O stretch

1655 cm⁻¹ : C=C stretch

(b)NMR

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The ratio is 9:18:2.

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