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lukranit [14]
4 years ago
12

1. Which is a chemical property of wood? conductivity flammability malleability

Chemistry
1 answer:
Allisa [31]4 years ago
3 0

Answer:

Wood consists mainly of organic substances (99% of the total mass). Elemental chemical composition of wood of different breeds is practically the same. Absolutely dry wood on average contains 49% of carbon, 44% of oxygen, 6% of hydrogen, 0.1-0.3% of nitrogen. When burning wood remains its inorganic part - ash.

So the answer is flammability because wood is flammable.

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During an experiment a thermometer was placed in a beaker containing hydrogen peroxide. The following observations were recorded
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The states of matter change to produce the same or the new substance. When yeast is added to hydrogen peroxide bubble of carbon dioxide is formed which indicates chemical change.

<h3>What is a chemical change?</h3>

A chemical change is the formation of a new substance by the chemical alterations in the reactants. The yeast releases products of cellular respiration that react with hydrogen peroxide.

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Phenol, c6h5oh, is a stronger acid than methanol, ch3oh, even though both contain an o]h bond. Draw the structures of the anions
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In resonance structures, the chemical connectivity in the molecule is same but the distribution of electrons are different around the structure.  They are created by moving electrons in double or triple bonds, and not atoms.

Phenol, C_6H_5OH and methanol, CH_3OH both are alcohols  that contain an -OH group attached to carbon atom.

Due to loss of 1 H from phenol, it forms phenoxide anion and due to presence of double bond in the benzene ring the negative charge on the oxygen atom (which represents electrons) will resonate with double bonds of benzene ring as shown in the image. The resonance-stabilized phenoxide ion is more stable. Whereas when methanol lose 1 H it forms methoxide anion and there are no such electrons present in the structure of methoxide that will result in the movement of electron. Since, due to resonance-stabilized phenoxide ion is more stable than methoxide ion, so it is a stronger acid.

The structures of the anions resulting from loss of 1 H from phenol and methanol is shown in the image.

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