QUESTION 4 What is the IUPAC name of this molecule? 5-methylpent-3-yne 2-methylp

Question

QUESTION 4 What is the IUPAC name of this molecule? 5-methylpent-3-yne 2-methylpent-3-yne S-methylhex-3-yne 2-methylhex-3-yne QUESTION 5 If the molecule above reacts with Br2/H2O following the patterns of electrophilic-addition mechanisms, which functional groups are in the product? One primary bromide, one secondary bromide, and two ketones One primary bromide, one secondary bromide, and two aldehydes Two primary bromides and two ketones Two secondary bromides and two ketones Two primary bromides and two aldehydes Two secondary bromides and two adehydes QUESTION 3 Which compound serves as an immediate precursor to the synthetic target shown below? QUESTION 1 Which tautomer is intermediate I, [I) best described by? Is it the keto or enol tautomer? QUESTION 2 What is the stereochemistry of the reaction using an alkali metal in liquid ammonia? Syn or Trans? For each mole of the molecule drawn, how many moles of hydrogen are added across each triple bond? Syn; 1 mole of hydrogen Trans; 1 mole of hydrogen Syn; 2 moles of hydrogen Trans; 2 moles of hydrogen

Explanation / Answer

Question 1)   enol

Question 2) trans ; 2moles of hydrogen

Question 3) D

Question 4) 2-methyl hex-3-yne

Question 5) two secondary bromide two ketone

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