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vovikov84 [41]
3 years ago
9

Which is stronger- the attractive forces between water molecules and chromium and chloride ions, or the combined ionic bond stre

ngth of CrCl2 and the intermolecular forces between water molecules? Explain?
Chemistry
1 answer:
Nutka1998 [239]3 years ago
6 0

Answer:

When chromium chloride, CrCl2, is dissolved in water, the temperature of the water decreases. ... The attractive forces between water molecules and chromium and chloride ions is stronger, because the reaction is endothermic means the energy released in formation is less than the energy required in breaking bond.

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How is wavelength measured (Select all that apply. from the trough (bottom) of one wave to the trough of the next wave
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Answer:

The first two

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Which criteria are responsible for deciding whether a heterogeneous mixture is a colloid or a suspension?
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What is the tool used for measuring volume?
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2 years ago
Write the chemical equation for fot the reaction between mgcl2 and the soap you preapred
In-s [12.5K]
Soap is the sodium or potassium salt of long chain of fatty acid. Fatty acids when treated with NaOH or KOH forms Soap. This process is called as Saponification. Examples of Soap are as follow,

                                     1.  Sodium Stearate C₁₇H₃₅COONa
                                   
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Reaction of Soap with MgCl₂;

When Soap is treated with MgCl₂ or CaCl₂ it forms insoluble precipitate called S.C.U.M. The reactions with MgCl₂ are as follow,

                2C₁₇H₃₅COONa + MgCl₂  -------->  2C₁₇H₃₅COOMg  + 2 NaCl

                2C₁₇H₃₃COOK   + MgCl₂  -------->  2C₁₇H₃₅COOMg  + 2 KCl

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5 0
3 years ago
In each reaction box place the best reagent and conditions from the list below benzene 3 boxes
den301095 [7]

Answer : The correct answer is 1) AlCl₃ - CH₃Cl 2) HNO₃ -H₂SO₄ at room temperature 3) Fuming HNO₃ -H₂SO₄ at 90-100 ⁰ C heat .

I think this reaction is forming 2,4,6- trinitrotoluene from benzene, since the product is not mentioned. Following are the steps to convert Benzene to 2,4,6 trinitrotoluene .

Step 1: Conversion of Benzene to Toluene .

Benzene can be converted to toluene by Friedel Craft Alkylation of benzene . In this reaction reagent AlCl₃ and Ch3Cl is used . Electrophile CH³⁺ is produced which attached on carbon of benzene and formation of Toluene and HCl occur.

Benzene     \frac{AlCl3}{Ch3Cl}>   Toulene + HCl

Step 2 : Conversion of Toluene to dinitrotoluene.

Dinitritoluene is prepared from toluene by Nitration . This reaction uses Electrophilic substitution mechanism . The reagents used are HNO₃ and H₂SO₄ at room temperature . These reagents produces NO₂⁺ ( nitronium ion ), a electrophile which attacks on C2 and C4 Carbon atoms of Toluene.

Toluene Tolune   \frac{HNO3 -H2SO4}{30-40 degree C} ->  2,4- dinitrotoluene

Step 3) Conversion of Dinitro toluene to trinitrotoluene.

This reaction is extended nitration of toluene . Further nitration is done in extreme condition . The temperature of reaction is increased to 90- 100 ⁰ C . Due to which there is more production of NO²⁺ ion occurs from HNO₃ -H₂SO₄ and they attack on C6 carbon atom of dinitrotoluene which forms 2,4,6- trinitrotoluene.

Dinitrotoluene 2,4 -dinitrotoluene   \frac{fuming HNO3-H2So4}{90-100 C} ->  2,4,6-trinitrotoluene.

So over all reaction uses three reagents in order :

Benzene  \frac{AlCl3}{CH3Cl}  -> Toluene  \frac{HNO3-H2So4}{room temp}  -> 2,4-dinitrotoluene  \frac{Fuming HNO3 -H2SO4}{Heating at 90-100 C}  -> 2,4,6-trinitrotoluene .

3 0
3 years ago
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