
(a)
Interpretation:
The practical method for the preparation of magnesium chloride from magnesium carbonate is to be determined.
Concept introduction:
A chemical equation refers to the symbolic representation of a given
(b)
Interpretation:
The practical method for the preparation of
Concept introduction:
A chemical equation refers to the symbolic representation of a given chemical reaction in the form of formulae and symbols where the product entities are present on the right hand side of the chemical equation while the reactant entities are present on the left hand side of the chemical equation.
(c)
Interpretation:
The practical method for the preparation of sodium sulfate from sodium chloride is to be determined.
Concept introduction:
A chemical equation refers to the symbolic representation of a given chemical reaction in the form of formulae and symbols where the product entities are present on the right hand side of the chemical equation while the reactant entities are present on the left hand side of the chemical equation.

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Chapter 21 Solutions
General Chemistry: Principles and Modern Applications, Loose Leaf Version (11th Edition)
- Synthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- If possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forward
- We mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forward
- Indicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forward
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