$\to_{H_{3} O +}^{{CH}_{3} MgBr (excess)}$ Product,

Product is:-

1.

2.

3.

4.

Subtopic: Aldehydes & Ketones: Preparation & Properties |

60%

1

2

3

4

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Q69:

Given the following reaction:

What is the structure of the product formed in this reaction?

1.		2.
3.		4.

Subtopic: Acid Derivatives - Preparation, Properties & Uses |

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Q70:

$\overset{HCN}{\to}$ A $\to_{(e x c e s s)}^{K C N}$ B;B is

1.

2.

3.

4.

Subtopic: Aldehydes & Ketones: Preparation & Properties |

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Q71:

Which shows decarboxylation by heating

1.

2.

3.

4.

Subtopic: Carboxylic Acids: Preparation & Properties |

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Q72:

The major product is
$\xrightarrow{LiAlH_4}$

1.		2.
3.		4.

Subtopic: Isomers & Reaction Mechanism |

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Q73:

Fehling solution gives red precipitated with

(a) Aromatic aldehyde

(b) Aliphatic aldehyde

(c) Ketone

(d) terminal $α$ -Hydroxy ketone

_{1. b,d}

_{2. a,b}

_{3. a,d}

_{4. b,c}

Subtopic: Aldehydes & Ketones: Preparation & Properties |

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Q74:

and can be distinguished by

1. I₂+NaOH

2. NaSO₃H

3. NaCN/HCl

4. 2,4-DNP

(1) a,b,d

(2) a,b

(3) a,c,d

(4) a,d

Subtopic: Aldehydes & Ketones: Preparation & Properties | Name Reaction |

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Q75:

$\to_{Zn / H_{2} O}^{O_{3} (I mole)}$ P $\to_{∆}^{NaOH}$ Q; Q is

1.

2.

3.

4.

Subtopic: Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |

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Q76:

$\overset{I_{2} + NaOH}{\to}$ x + y(yellow ppt) y $\to_{∆}^{Ag}$ z;z is

1. CH $\equiv$ CH

2. CHI₃

3. Ph-COONa

4. CH₂=CH₂

Subtopic: Aldehydes & Ketones: Preparation & Properties |

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Q77:

$\to_{ii \cdot ∆}^{i \cdot K_{2} {Cr}_{2} O_{7}}$ X; X is

1.

2.

3.

4.

Subtopic: Aldehydes & Ketones: Preparation & Properties |

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$\to_{H_{3} O +}^{{CH}_{3} MgBr (excess)}$ Product,

Product is:-

1.

2.

3.

4.

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→H3O+CH3MgBrexcessProduct, Product is:- 1. 2. 3. 4.

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$\to_{H_{3} O +}^{{CH}_{3} MgBr (excess)}$ Product,

Product is:-

1.

2.

3.

4.