Can you show how a sulfonic acid group is introduced into an aromatic ring by Friedal Craft Rxn using CHEM DRAW only. please don't bother answering this problem if it is not using Chem draw :)
Can you show how a sulfonic acid group is introduced into an aromatic ring by Friedal...
2. Not only does an aromatic ring itself affect the reactivity of an acid derivative (an ester, on last year's quiz), substituents on the aromatic ring can further modify the reactivity. First, we will consider a phenyl amide with a para-acetyl substituent: CH, (a) What is the n-effect (resonance) of the para-acetyl substituent? How will that affect the reactivity of the other (amide) carbonyl in the molecule below (increase or decrease, compared to the same amide but with no p-...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
organic. how would you add a phenyl group to a benzene ring? please show the mechanism and steps (hint was to use grignard)
can you please help me figure out my unknown no, it is part of what i am trying to figure out. Based off of solubility and functional group testing it is a weak acid/ phenol and aromatic
please answer every part of question 6!! and i will make sure to thumbs up the answer! 6) a) How many aromatic 'H NMR signals would be expected for 4-bromo-3-methylanisole? (0.5 pts.) b) What would the expected 'H NMR chemical shift be for the protons of the OCH; group?_ _(0.5 pts.) c) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H. through H., if needed. If the hydrogens are chemically shift...
How can you tell you have an aldehyde instead of ketone? or caboxylic acid? How can you distinguish between primary, secondary and tertiary amines? How can you distinguish between nitrile (CN) and alkyne? How can you distinguish between aromatic double bond vs non-aromatic double bonds? What's the different between alcohol OH and carboxylic acid OH? What's the different between sp2 CH vs sp3 CH?
5. Glucose can form two different ring structures as shown. Draw a mechanism to show how each is formed (don't worry about the stereochemistry around the anomeric carbon) он CHO HO HO он OH но OH он pyranose form of D-glucose OH CH2OH HO D-glucose HO но он он furanose form of D-glucose
7. Using resonance structures show how the amino group would effect the electron density on the ring carbons of the following compound. Would you expect an electrophile to attack this molecule at the ortho, meta or para position(s)? 8. Draw the structure of (3R, 4R)-3-(3-fluorophenyl)-4-formylhexan-2-one ing resonance structures, show how the amino group would effect the electron density on the ring carbons of the following compound. Would you expect an electrophile to attack this molecule at the ortho, meta or...
please answer every part of number 8, i will thumbs up answer! 8) a) How many aromatic 'H NMR signals would be expected for 2-bromo-5-methylanisole? (0.5 pts.) b) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H, through H , if needed. If the hydrogens are chemically shift equivalent, use the same label for each member of the set of equivalent hydrogens. ΥΗ c) Calculate the chemical shifts for the aromatic...
You can work in a small group with classmates to share your approach and problem solving. However, each student must submit their individual work. All explanations require several full sentences 1. Rank these carbonyl compounds from one to five (5 being the least electrophilic) in their ability to serve as electrophiles in a nucleophilic acyl addition. Then explain your ranking in several sentences المد الا 2. Rank these aromatic compounds from one to five (5 being the least nucleophilic) in...