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Federal (FBISE) · Chapter test · Free

1st Year Chemistry Chapter 21 Test21. Organic Synthesis

30 marks · 40 minutes · 21 questions. Covers: 21. Organic Synthesis.

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1st Year Chemistry Chapter 21 Test

1st Year · Chemistry · Federal (FBISE)

Name: ____________Roll No: ________Class/Section: ________Date: ________Total marks: 30Time: 40 minutes

Q1. Multiple choice questions (Attempt all · 10 × 1 = 10)

  1. The function of Al₂O₃ or concentrated H₂SO₄ is to:
    1. Oxidize alcohols
    2. Form esters
    3. Add hydrogen to double bonds
    4. Remove water from a molecule
  2. Retrosynthesis is the process of:
    1. Combining simple reactions to make a compound
    2. Distilling alcohols
    3. Separating organic mixtures
    4. Breaking a target compound into simpler precursors
  3. Retrosynthesis works in which direction?
    1. Forward direction
    2. Backward from target to precursor
    3. Random reaction sequence
    4. Simultaneous pathway
  4. Retrosynthetic analysis is also known as:
    1. Deconstruction
    2. Dehydration
    3. Oxidation
    4. Hydrolysis
  5. The reaction scheme outlines the production of one of the monomers of nylon 66 from compound X. {Compound X →KCN in ethanol → NCCH2CH2CH2CCH2CNNCCH_2CH_2CH_2CCH_2CN → reduction→H2N(CH2)H_2N(CH_2)6NH26NH_2.}Which compound could be?
    1. BrCH2CH2CH2CH2BrBrCH_2CH_2CH_2CH_2Br
    2. CH2=CHCH=CH2CH_2=CHCH=CH_2
    3. HOCH2CH2CH2CH2OHHOCH_2CH_2CH_2CH_2OH
    4. HO2CCH2CH2CH2CH2CO2HHO_2CCH_2CH_2CH_2CH_2CO_2H
  6. The condition required for free radical substitution is:
    1. Diffused sunlight
    2. Darkness
    3. High pressure
    4. Acidic medium
  7. The reagent used for elimination reaction of alkyl halides is:
    1. NaOH (aqueous)
    2. NaOH (ethanolic)
    3. HCl
    4. H₂SO₄
  8. Butanedioic acid may be synthesised in two steps from 1,2-dibromoethane BrCH2CH2Br→Step1→X→Step2→HO2CCH2CH2CO2H{BrCH_2CH_2Br → Step 1 → X → Step 2 → HO_2CCH_2CH_2CO_2H} Which reagents could be used for this synthesis?
    1. Step 1: HCN(g) Step 2: HCL(aq)
    2. Step 1:HCO2NaHCO_2Na(aq) Step 2:HCL(aq)
    3. Step 1:KCN(aq/alcoholic) Step 2: H2SO4H_2SO_4(aq)
    4. Step 1:NaOH(aq) Step 2: K2Cr2O7/H2SO4(aq)K_2Cr_2O_7/H_2SO_4(aq).
  9. The iodoform test gives a yellow precipitate of:
    1. CHI₃
    2. CHCl₃
    3. CH₂I₂
    4. CO₂
  10. Alkyl halides undergo which reactions?
    1. Nucleophilic substitution and elimination
    2. Addition and oxidation
    3. Substitution and reduction
    4. Oxidation and esterification

Q2. Short questions (Attempt any 6 of 8 · 6 × 2 = 12)

  1. How can you identify chloroalkane using silver nitrate test?
  2. Define retrosynthesis.
  3. What products are formed during ozonolysis of alkene?
  4. Which two fragments are obtained in the retrosynthesis of ethyl propanoate?
  5. How are alkenes oxidized to diols?
  6. What is free radical substitution?
  7. Write the color of precipitate formed in 2,4-DNP test.
  8. Write the structure of ethyl propanoate.

Q3. Long questions (Attempt any 2 of 3 · 2 × 4 = 8)

  1. Discuss important organic reactions shown by alkanes, alkenes, alkyl halides, alcohols, carbonyl compounds, and carboxylic acids with examples.
  2. Compare and contrast between synthesis and retrosynthesis.
  3. Samples of the following compounds were labelled A to E as shown. (A) CH₃CH₂CH₂OH (B) CH₃CH₂CH(OH)CH₃ (C) CH₃CHO (D) CH₃COCH₃ (E) CH₃CH=CHCH₃ Complete the table below by inserting the letter (or letters) of the compounds that correspond to each test.