(a)
Interpretation:
Michael donor and Michael acceptor need to be identified for the given set of compounds.
Concept introduction:
When a active methylene is deprotonated to form a carbanion (Michael donor) which acts as a nucleophile for 1,4-conjugate addition to
Please remember that 1,5-difunctionalization is the hallmark of Michael addition reaction.
To Find : To find the Michael donor and Michael acceptor for the given compound.
(b)
Interpretation:
Michael donor and Michael acceptor need to be identified for the given set of compounds.
Concept introduction:
When a active methylene is deprotonated to form a carbanion (Michael donor) which acts as a nucleophile for 1,4-conjugate addition to
Please remember that 1,5-difunctionalization is the hallmark of Michael addition reaction.
To Find : To find the Michael donor and Michael acceptor for the given compound.
(c)
Interpretation:
Michael donor and Michael acceptor need to be identified for the given set of compounds.
Concept introduction:
When a active methylene is deprotonated to form a carbanion (Michael donor) which acts as a nucleophile for 1,4-conjugate addition to
Please remember that 1,5-difunctionalization is the hallmark of Michael addition reaction.
To Find : To find the Michael donor and Michael acceptor for the given compound.
(d)
Interpretation:
Michael donor and Michael acceptor need to be identified for the given set of compounds.
Concept introduction:
When a active methylene is deprotonated to form a carbanion (Michael donor) which acts as a nucleophile for 1,4-conjugate addition to
To Find : To find the Michael donor and Michael acceptor for the given compound.
(e)
Interpretation:
Michael donor and Michael acceptor need to be identified for the given set of compounds.
Concept introduction:
When a active methylene is deprotonated to form a carbanion (Michael donor) which acts as a nucleophile for 1,4-conjugate addition to
Please remember that 1,5-difunctionalization is the hallmark of Michael addition reaction.
To Find : To find the Michael donor and Michael acceptor for the given compound.
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- Choose the option that is decreasing from biggest to smallest. Group of answer choices: 100 m, 10000 mm, 100 cm, 100000 um, 10000000 nm 10000000 nm, 100000 um, 100 cm, 10000 mm, 100 m 10000000 nm, 100000 um, 10000 mm, 100 cm, 100 m 100 m, 100 cm, 10000 mm, 100000 um, 10000000 nmarrow_forwardQ1. (a) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH3. Use curved arrows to show the electron movement. (b) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH4*. Use curved arrows to show the electron movement.arrow_forwardWhich is NOT the typical size of a bacteria? 1000 nm 0.001 mm 0.01 mm 1 umarrow_forward
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