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yawa3891 [41]
3 years ago
14

Is iron bromide magnetic if no why

Chemistry
2 answers:
Nataly_w [17]3 years ago
4 0
Iron bromide isn't considered magnetic because all iron compounds  are not magnetic 
Mila [183]3 years ago
3 0

Answer:

Yes, Iron bromide is magnetic.

Explanation:

Iron bromide is a chemical compound with chemical formula FeBr2. It is a anhydrous compound with yellow and brownish color paramagnetic solid. Iron is magnetic. So, any metal with iron will be attracted to a magnet. Some metals like copper, gold and aluminium are non-magnetic.

Not all iron is magnetic. Iron is a ferromagnetic which is attracted to the magnets like nickel and cobalt. It is non-magnetic because they have net dipole moment of  zero and have partially field electron shell.

Iron bromide is magnetic because it possses the strong magnetism at 4.2 degree kelvin.

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Given the balanced ionic equation:
bezimeni [28]

Answer : The correct option is, (4) 6.0 mol

Explanation :

The given balanced chemical equation is,

3Pb^{2+}+2Cr\rightarrow 3Pb+2Cr^{3+}

In this reaction, lead undergoes reduction and chromium undergoes oxidation.

Oxidation reaction : It is the reaction in which a substance looses its electrons. In this oxidation state increases.

Reduction reaction : It is the reaction in which a substance gains electrons. In this oxidation state decreases.

Half reactions of oxidation-reduction are :

Oxidation : 2Cr\rightarrow 2Cr^{3+}+6e^-

Reduction : 3Pb^{2+}+6e^-\rightarrow 3Pb

From the reduction reaction, we conclude that 6 moles of electrons gained by the 3 moles of lead ions.

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5 0
3 years ago
Benzene and alkyl-substituted benzenes can be hydroxylated by reaction with H2O2 in the presence of an acidic catalyst. What is
Yuri [45]

Answer:

The electrophile is the hydroxide free radical

Explanation:

The hydroxylation of benzene and benzene derivatives using hydrogen peroxide proceeds in the presence of an acidic catalyst. The electrophile in this reaction is the hydroxyl free radical generated in an initial step of the reaction.

This is actually a free radical reaction. The hydroxyl radical previously generated reacts with the benzene ring to yield a radical that undergoes further rearrangement to yield the product phenol. The intermediate, shown as part of this reaction mechanism (refer to image attached) is a specie in which the odd electron is delocalized over the entire benzene ring. Loss of a proton completes the reaction mechanism yielding the corresponding phenol.

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4 years ago
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alekssr [168]

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6 0
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4 years ago
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saveliy_v [14]

Answer:

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