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Practice Exercise 1



This activity contains 6 questions.

Question 1
1 How is a formyl substituent (-CH=O) on a ring denoted in systematic nomenclature?
 
End of Question 1


Question 2
2 How many carbons are there in isohexyl methyl ketone?
 
End of Question 2


Question 3
3 Which of the following compounds is the least reactive towards nucleophilic attack?
 
End of Question 3


Question 4
4 What product is formed from the reaction of an aldehyde with a Grignard reagent followed by addition of H+/H2O?
 
End of Question 4


Question 5
5 What Grignard reagent is needed to prepare pentanoic acid from the reaction of a Grignard reagent with carbon dioxide?
 
End of Question 5


Question 6
6 Carbonyl compounds can be reduced to alcohols using sodium borohydride followed by addition of H+/H2O. Which statement best describes the mechanism?
 
End of Question 6


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