Queston 3 Indicate any of the following that are aromatic. (More than one answer) Overall G
aromatic amines are mor more basic the amine of aniline
Aromatic amines are more basic than the amine of aniline if NH2 aniline Select one: The nitrogen lone pair is part of a sulfonamide, The nitrogen has a positive charge as in a quaternary amine. The nitrogen lone pair is involved in resonance with a carbonyl group. The aromatic ring is substituted with electron donating groups. The aromatic ring is substituted with electron withdrawing groups. Choose the correct product for...
2. (3 pts) Indicate if the compounds shown below would be predicted to be aromatic, non-aromatic, or anti-aromatic if they had a planar structure. :5; NCHE 3. (3 pts) Rank the following compounds in order of reactivity with Bry in the presence of FeBrs. DDD Chay Least Reactive Most Reactive
**draw product(s) of the following E1 reaction. if there is
more than one possible product, indicate which is the major and
which is the minor product.
Question 27 2 pts **WRITTEN WORK** Draw the product(s) of the following El reaction. If there is more than one possible product, indicate which is the major and which is the minor product. носн, ΕΙ HTML Editore BIVA I E333xx, 12pt 2 Paragraph 1 words р 1 te
Which of the following substituted benzene rings is more
activated towards electrophilic aromatic substitution than benzene?
Select all that apply
Which of the following substituted benzene rings is more activated towards electrophilic aromatic substitution than benzene? Select all that apply. CF3 Br NH2 OH A 00 D E F ОЕ OF D ОА OB Ос
predict the product(s) for the following reactions.
Indicate proper stereochemistry when needed. if more than one
stereoisomer forms, draw each one separately.
H2 Pd-C m-CPBA CH2CI NaBH4 CH3OH 1) NaH 2) CH3Br 3) H2 / Lindlar catalyst
Draw Louis structures for the following molecules.each molecule has
more than one central atom. use supplied hints to arrange atoms
into molecular framework then fill in the blank. for bond
polarities, indicate the polar bonds on your Lewis structures using
the S+ and S- notation.
Experiment 8 Part 2: Molecules and lons with More Than One Central Atom Molecular geometries (indicate which atom): N₂F4 Ideal bond angles (indicate which atom): Are polar bonds present? (Indicate on Lewis dot structure.) Is...
Draw the products of the following reactions. If more than one
product is expected, indicate which would be the major product, if
predictable. Include stereochemistry where relevant.
NaOET NaO Me t-BUOK NaSH NaOEt NaOH
2. For each of the following expressions, indicate which (if any) of the following apply (more than one may apply) and list how many literals each expression has: i ii Product Term SOP expression Sum Term POS Expression iv. a. ABD b. A'B + AD c. (A + D')(C+ ABD) d. A + B' e. (A+B')(B+C)(A'+C+D')
there should be more than one answer
Question 3 1 pts One of the observed effects of relativistic travel is length contraction. Which of the following statements describes how an observer experiences length contraction? The observer measures objects that move past them as shorter than if they were at rest. No objects actually change size The observer measures a change in all three spatial dimensions Bength width and height of an object that they move past The observer measures that...
MULTIPLE ANSWER CHOICES ARE POSSIBLE (more than one correct)
Question 7 Which of the following statements are true about the deactivating nitroso substituent in electrophilic aromatic substitution reactions? NFO The nitroso group is predicted to be an ortho/para-directing group. Resonance withdrawing effects can explain why the nitroso group is deactivating. The nitroso group is predicted to be an meta-directing group. Inductive withdrawing effects can explain why the nitroso group is deactivating.