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ElenaW [278]
3 years ago
11

Name three chemical properties of wood

Chemistry
1 answer:
Zielflug [23.3K]3 years ago
4 0

Answer:

Burn, able to rust, and sour.

Explanation:

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12. What is the name of the compound MnF,? (Chapter 9)
nordsb [41]

Answer: D

Explanation:

3 0
3 years ago
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Rank the members of each set of compounds in order of decreasing ionic character of their bonds. Use partial charges to indicate
Firdavs [7]

Answer:

Ionic character

A.  PF₃ > PBr₃ > PCl₃

B. BF₃ > CF₄ > NF₃

C. TeF₄ > BrF₃ > SeF₄

Explanation:

The most electronegative element is fluorine, followed chlorine, phosphorous nitrogen etc.

  • Atoms with high electronegativity tend to form negative ions.
  • Ionic compounds formed between elements with high electronegativity difference.
  • % ionic character is directly proportional to electronegativity difference.
  • According to Pauling Scale E.n for F(4.0), O(3.5), N(3.0), C(2.5), B(2.0), P(2.19), Se(2.55) , Te (2.1), Cl(3.16) and Br(2.96)
  • ΔE.N (Electronegativity difference) between( P and F = 4 - 2.19 = 1.81), (P and Br = 2.96 - 2.19 = 0.77) , (P and Cl = 3.16 - 2.96 = 0.2 )
  • ΔE.N (Electronegativity difference) between( N and F = 4 - 3 = 1), (B and F = 4 - 2 = 2) , (C and F = 4 - 2.5 = 1.5 )
  • ΔE.N (Electronegativity difference) between( Se and F = 4 - 2.55 = 1.45), (F and Te = 4 - 2.1 = 1.9) , (F and Br = 4 - 2.19 = 1.81 )

6 0
3 years ago
What is the radius of a circle i<br>s ​
Nonamiya [84]

Answer:

The Radius is the distance from the center outwards. The Diameter goes straight across the circle, through the center. The Circumference is the distance once around the circle.

6 0
3 years ago
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Draw the most stable resonance structure for the intermediate in the electrophilic aromatic bromination of aniline, anisole, and
ASHA 777 [7]

Answer:

Here's what I get

Explanation:

(a) Intermediates

The three structures below represent one contributor to the resonance-stabilized intermediate, in which the lone pair electrons on the heteroatom are participating (the + charge on the heteroatoms do not show up very well).

(b) Relative Stabilities

The relative stabilities decrease in the order shown.

N is more basic than O, so NH₂ is the best electron donating group (EDG) and will best stabilize the positive charge in the ring. However, the lone pair electrons on the N in acetanilide are also involved in resonance with the carbonyl group, so they are not as available for stabilization of the ring.

(c) Relative reactivities

The relative reactivities would be

C₆H₅-NH₂ >  C₆H₅-OCH₃ > C₆H₅-NHCOCH₃

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3 years ago
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