Description

The resonance effect makes a carbonyl compound ______ reactive towards a nucleophile
Mixture of products formed in Sn1
An aldehyde is ____ reactive than a ketone
Shows a map of C-H framework
T/F: An amide can be converted into an ester
A poor nucleophile and a strong base will favor _____
Happens as a result of an umbrella flip in Sn2
Heat favors _____
Methyl Hs (attached to the same C) are _____
The resonance effect is very effective with N and O as Y groups because the _____ are similar in size
What is the stereochemistry of E2 reactions?
The lower the ______ the more nucleophilic
Poor nucleophiles generally have a _____ charge
High steric strain _______ nucleophilicity
Hydrogen on Oxygen, Nitrogen, or Halogens
Large bases in E2 reactions form _____ products
What is the least reactive Y group?
A good nucleophile and a weak base will favor ______
OH is an _____ group
An acid chloride has ______ reactivity than an acid anhydride
When molecules are radiated with ______ the bonds bend, wag, and stretch
The most reactive Y group is _____
Weak bases (conjugate) bases of strong acids) are _________
Can show functional groups present in a molecule
Good nucleophiles generally have a _____ charge
A poor nucleophile and a strong base will favor _____
The inductive effect makes a carbonyl compound _____ reactive towards a nucleophile
E1 reactions most often form _____ products
_____ will convert an amide to an amide

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Frequently Asked Questions

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Some of the words will share letters, so will need to match up with each other. The words can vary in length and complexity, as can the clues.

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If this is your first time using a crossword with your students, you could create a crossword FAQ template for them to give them the basic instructions.

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