(b) Please draw the structures of (i) meta-chlorobenzoic acid, (ii) meta-ethylbenzoic acid, and (ii) para-hydroxy methyl...
Part II: disubstituted benzene derivatives 5. Give two names, one with numbered substi one with numbered substituents, the other with ortho, meta or para designations, for each of the following benzene derivatives: OH CH3 U niw olla 6. Draw structures for the following: a. O-chlorobenzoic acid C. m-bromophenol erilisator Somnold. d ansulotorola Somosd-ES b. p-dinitrobenzene d. 1-bromo-4-chlorobenzene
Name the following compounds according to the IUPAC system. (i) (ii) Draw out of structures for the following compounds (i) 5-Methyl-2-naphthalenesulfonic acid (ii) 8-Nitronthracen-1-ol
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Liy myas iw nolt yd fuods Name: anibia blsu base loro o done Part I: single substituents Lab report for lab the week of October 22 1. What is the name of the compound with the formula CsHsBr? What is the special name of the compound with the formula CeHsCH3?- 2. 3. What is the special name for benzene with an amino group attached to the ring? 4. What is the special name for the benzene derivative with an alcohol...
JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH a) NO2 b) CI c) 4-phenyl-2-pentanol; •DH d) 1-bromo-2-chloro-4-ethylbenzene; 2. Arrange the compounds in each set in order of decreasing reactivity (fastest to slowest) toward EAS. Explain. (2 pts) 0-C-CH3 -C-0-CH3 a) (A) (B) (C) CH2CH3 -NH2 ( C1) do nosotros (B) b) (A) 3. Account for the observation that trifluoromethyl groups is meta directing, as shown in the following example. (1 pt) CF3...
please explain both in the simpliest way im lost 4. Draw missing resonance structures in the boxes below Curved arrows are not required. H Organic compounds can serve as Bronsted-Lowry acid in water. The degree of deprotonation in aqueous solution depends 5. Acetaminophen is the active ingredient in Tylenol® and is insoluble in water. However, its deprotonated form is soluble in on the strength of the acid (pKa) and the pH of the aqueous solution. water when strong enough base...
i)Draw bond-line structures for each of the following: [4 marks] a) 2-butyloxiraneo ZWn c) 2-methyl-3-hekyn-2-ol b) Ethylhexanoate d)2-chloro benzoic acid
Draw the structures of the following organic compounds a) 2,4-dicholoroheptane b) 2,2-dicholorohexane c) 2-methyl-4-ethylnoname d) 2,2,4-trimethyldecane e) 2-methyl-3-isoprophylheptane f) 1-methylcyclohexane g) 1,1-diethylcyclopentane h) 1-bromo-2-methylcycloheptane i) 1,2-dichlorocyclobutane
Which one of the following is the s-sis conformation of (Z-2-methyl-2,4-hexadiene? oyna on synd or Rank the following compounds in order of decreasing reactivity to aromatic electrophilic bromination A. benzene B. toluene C. benzoic acid D. phenol 1)D>B>A>C 2)D>C>B>A 3) B>A>D>C 4)B>>D>A Which of the following is the aromatic compound? 1) 2) Which of the following ions are anti-aromatic species? Å А B D 1) A and D 2) Band 3) B and D 4) Cand D What is (are)...
I. name the following compounds II. write structures for each of the followong structires III.Arrange alkenes from most to least stable IV. if rearrangement is expected, draw rearranged structure for wach carbocation V. PLEASE HELP, ive been struggling in organic and this is the review for our 3rd exam. if i can get help (and explanations) for 1-4 it would be a big help CHM 2210 Examination 3 11/02/18 Directions: Please supply all answers in the spaces provided on both...