
(a)
Interpretation:
Structural formula of thioformaldeyde has to be drawn.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom.
If either of the carbon atom or the oxygen atom present in the carbonyl group is substituted by sulfur atom means it is known as sulfur-containing carbonyl compounds.
(b)
Interpretation:
Structural formula of methanethial has to be drawn.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
If either of the carbon atom or the oxygen atom present in the carbonyl group is substituted by sulfur atom means it is known as sulfur-containing carbonyl compounds.
(c)
Interpretation:
Structural formula of thioacetone has to be drawn.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
If either of the carbon atom or the oxygen atom present in the carbonyl group is substituted by sulfur atom means it is known as sulfur-containing carbonyl compounds.
(d)
Interpretation:
Structural formula of propanethione has to be drawn.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
If either of the carbon atom or the oxygen atom present in the carbonyl group is substituted by sulfur atom means it is known as sulfur-containing carbonyl compounds.

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Chapter 15 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Please help me solve this reaction.arrow_forwardIndicate the products obtained by mixing 2,2-dimethylpropanal with acetaldehyde and sodium ethoxide in ethanol.arrow_forwardSynthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- 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
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