Consider the given reaction: 
\(\mathrm{CH}_3 \mathrm{COCH}_3 \stackrel{\mathrm{dil.~Ba}\left(\mathrm{OH)}_2\right.}{\longrightarrow} \text { " } \mathrm{X} "\)
The functional groups present in the compound "X" are: 

1. Ketone and double bond 
2. Double bond and aldehyde 
3. Alcohol and aldehyde 
4. Alcohol and ketone 

Subtopic:  Name Reaction |
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Mark the name of the reaction associated with the following conversion


1. Stephen reaction 
2. Gattermann-Koch reaction 
3. Etard reaction 
4. Rosenmund reaction 
Subtopic:  Name Reaction |
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Identify the product in the following reaction:
 
1. 2.
3. 4.
Subtopic:  Name Reaction |
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The following reaction is one of many steps in the laboratory synthesis of cholesterol. What type of reaction is it? 
 
1. Reduction reaction. 
2. Oxidation reaction. 
3. Catalytic hydrogenation. 
4. Electrophilic substitution. 
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Nitriles are hydrolyzed to amides upon mild heating with an aqueous base or acid. The product of hydrolysis under stronger conditions is: 
1. Aldehyde  2. Ketone 
3. Ester  4. Carboxylic acid 
Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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The hemiketal of acetone can be formed by adding: 

1. HCl 
2. CH3OH
3. NaOH
4. Formaldehyde
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Identify the final product [D] obtained in the following sequence of reactions:

 
1.  \(\mathrm{HC\equiv C^-~Na^+}\) 2.
3. 4. \(\mathrm{C_4H_{10}}\)
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Identify the major product obtained in the following reaction: 
1. 2.
3. 4.
Subtopic:  Name Reaction |
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Identify the product (A) in the following reaction: 
1.
2.
3.
4.
Subtopic:  Name Reaction |
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Given is a reaction for your reference:

The final product [C] is:
1. 2.
3. 4.
Subtopic:  Aldehydes & Ketones: Preparation & Properties | Carboxylic Acids: Preparation & Properties |
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