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4 years ago

How is carbon dioxide formed

1 answer:

3 0

Carbon dioxide is produced by any living creature such as ourselves when or plants during the process of respiration. Carbon dioxide is also produced by humans when we burn fossil fuels, ie running our cars or burning gas, coal or oil for energy.

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Which of the following is a type of cell organelle?

icang [17]

Answer:

C . Dna

Explanation:

8 0

3 years ago

True or false: Most of the mass of an atom is found in the electron layers.

Nataly_w [17]

I wanna say false, but I’m sorry if I’m wrong :(

3 0

3 years ago

Using the following thermochemical equation, determine the amount of heat produced from the combustion of 24.3 g benzene (C6H6).

Anna007 [38]

Answer:

ΔH = -976.5 kJ

Explanation:

For the reaction given, there are 2 moles of benzene (C6H6). The heat of this reaction is -6278 kJ, which means that the combustion of 2 moles of benzene will lose 6278 kJ of heat. It is an exothermic reaction.

The value of ΔH, the enthalpy, is a way of measurement of the heat, and it depends on the quantity of the matter (number of moles).

So, 24.3 g of benzene has :

n = mass/ molar mass

n = 24.3/78.11

n = 0.311 moles

2 moles ------------ -6278 kJ

0.311 moles ----------- x

By a simple direct three rule:

2x = -1953.08

x = -976.5 kJ

3 0

3 years ago

When KCl dissolves in water:

34kurt

This dissociation occur because:

O had to bond with H due to the Hydrogen bonding rule, which will form OH~ (Hydroxide).

K is more attracted to Hydroxide than Cl, so it will depart Cl and bond with OH~.

that leaves a H and a Cl, which one has a positive charge and the other has a negative, so they will bond and form Hydrochloric Acid.

3 0

3 years ago

(a) How many stereoisomers are possible for 4,4-dimethyl-1,2-cyclopentanediol?

Monica [59]

Answer:

(a) 4 stereoisomers: (1R,2S) 4,4-dimethylcyclopentane1,2-diol; (1R,2S) 4,4-dimethylcyclopentane1,2-diol; (1S,2S) 4,4-dimethylcyclopentane1,2-diol; (1R,2R) 4,4-dimethylcyclopentane1,2-diol. (b) (1R,2S) 4,4-dimethylcyclopentane1,2-diol; (1R,2S) 4,4-dimethylcyclopentane1,2-diol (c) No, they are optically inactive.

Explanation:

(a) The stereoisomers possible for 4,4-dimethyl-1, 2-cyclopentanediol are (1R,2S) 4,4-dimethylcyclopentane1,2-diol; (1R,2S) 4,4-dimethylcyclopentane1,2-diol; (1S,2S) 4,4-dimethylcyclopentane1,2-diol; (1R,2R) 4,4-dimethylcyclopentane1,2-diol. Their structures are shown in the attached file.

(b) The oxidation reaction that occurs between 4,4-dimethylcyclopentene and osmium tetroxide produces (1R,2S) 4,4-dimethylcyclopentane1,2-diol; (1R,2S) 4,4-dimethylcyclopentane1,2-diol. Their structures are also shown in the attached file.

(c) The products of the oxidation reaction in (b) are optically inactive because the compounds contain plane of symmetry that makes them optically inactive compound.

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4 years ago