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Basic Organic Chemistry

Created by karen_rx

Fun Trivia : Quizzes : Organic Chemistry
Basic Organic Chemistry game quiz
"This requires a good amount of education in organic chemistry, but any second semester student should be able to answer the following questions. They are fairly simple, not meant to be tricky or difficult in any way. Good luck!"

15 Points Per Correct Answer - No time limit  



1. Which of the following types of reactions involves R-X, Li, CuI, and R'-X?
    Clemmenson Reduction
    Corey-Posner , Whitesides-House synthesis
    Friedel-Crafts Alkylation
    Grignard synthesis


2. In the type of reaction involving R-X, Li, CuI, and R'-X?; R'-X must NOT be which of the following?
    Primary
    Secondary cycloalkyl
    Methyl
    Tertiary


3. Grignard reagents react with ketones to form which of the following?
    Tertiary alcohols
    Secondary alcohols
    Primary alcohols
    Carboxylic acids


4. Which of the following is a Huckel number?
    10
    12
    8
    16


5. Which of the following are reagents used in the nitration of benzene?
    Concentrated NO3
    Dilute solutions of NO3 and H2SO4
    Conc. HNO3 and conc. H2SO4
    Ammonia


6. Which of the following is NOT associated with oxidation?
    PCC
    LiAlH4
    Jones Reagent
    Hot KMnO4


7. Which of the following will reduce an aldehyde but not a carboxylic acid?
    NaBH4
    H2, Pt catalyst
    LiAlH4
    PCC


8. If branching of the side chain in the product is a problem in Friedel-Crafts alkylation, how can a product with an unbranched side chain be reached?
    Use Cl2 instead of AlCl3
    It can't--the more stable carbocation cannot be avoided
    Friedel-Crafts acylation followed by Clemmenson reduction
    Treat the product with a strong acid


9. A methyl group on benzene is considered which of the following?
    Ortho-para director, deactivating
    Ortho-para director, activating
    Meta director, activating
    Meta director, deactivating


10. When an alcohol is exposed to an acid, what is the first thing that always happens?
    Protonation of the hydroxyl group
    A double bond forms
    An acid-base reaction
    It becomes a diol

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