1.
a) 3-oxopropanoyl chloride
Reason;
COCl is highest priority and suffix is 'oyl chloride' there are 3 carbon so propan as parent chain. prefix of aldhehyde group is oxo and it is at 3 position so 3-oxopropanoyl chloride.
b) 2-hydroxypropanedinitrile
Reason; Nitrile group has highest priority and alcohol is lowest priority so numbering done from CN. Parent chain is of 3 carbon including 2 nitrile group so propanedinitrile.
c) 4-hydroxy-3-methoxybenzaldehyde
Reason; the parent chain is benzene and the highest priority is aldehyde group so benzaldehyde and numbering done from aldhehyde so at 3 position is methoxy and 4 is hydroxy group.
d) 3-amino-4-((1-methoxy-1-oxo-3-phenylpropan-2-yl)amino)-4-oxobutanoic acid
Reason; the highest priority is carboxylic acid so numbering is done from that point. At 3 position is amino and at 4 position there is one amino group & one propanyl chain attached so in propanyl chain at 3 position is phenyl ring. In this propanyl chain numbering is done from carbonyl carbon.
1. Write the IUPAC of the following structures : (12 points) HOCCHCOCI 6) (CN)2 CHOH i...
write the IUPAC name of each of the following , using cis or trans
prefixes
6. CH₂ D. 113 H volt c-C non so H CH-CH2-CH-CH2 who n g c. CH3-CH2-CH, Ho C=C H CH2-CH3
3. . Draw all the possible resonance
structures: (6 points)
4. Write the products or reactants: (12
points)
3.. Draw all the possible resonance structures: (6 points) OCH3 H NO2 a. CH2 CH + H3C CH2 b. H,C 4. Write the products or reactants: (12 points) COOH 0-1 heat COOH a. HBr, leq b.
1. For each of the following structures, i. write the IUPAC name. (2 pts.) ii. classify each halogen as 1º, 2º, or 3º. (1 pt.) 2. Draw structures for the following alkyl halides. Be sure to indicate any stereochemistry as needed. (2 pts. each) a. 3,6-dibromo-3,6-dichlorononane b. 2-iodo-2-methylpentane Page 3 4. Indicate which alkyl halide you would expect to react more rapidly by an S12 mechanism. (2 pts.) Explain your answer. (2 pts.) 3. i. State which reagent you would...
Give the IUPAC name of each of the following compounds
aromate D) amine E) ketone 2. Give the IUPAC name of each of the following compounds: H OH HC (a) Hoc (b) CHE (c) Hoc HO (d) CH3 CHE HC (e) Ho-o (1) na CH₂ H CH₂ HyC N. CH3 HC N ( g ) сн.
5. Which of the following structures is an isomer of the compound in the box? CHE Chu-Chi-CH-CH-CH, A CH:CH-CH2 - CH2 B. CH, CH CH үн. CH-CH-CH-CHECK to the CH сна C. 8_5-8 CH-CH2CH сна D. CHECH-CH2-CH-CH3 1 CHE CHE 6. Determine the following pairs whether they are conformational isomers, structural (constitutional) isomers, optical isomers, geometric isomers, or not isomers. A. B. OH c. D. E F. H G. H. HO I J. K. L.
a 5). Write the products for the jonization of the following carboxylic acids in 1. CH3-CHz-6-0H+H0 = ..OH + H₂O 2. benzoic acid + H2O = 0 Write the products and names for each of the following reactions: 1.o + xood – 1. CH-CH2-C-OH + NaOH - Okt 2 comic nie + KOH - A lok - A-cookt Write the products of the following reactions: 1. CH ----OH + CH2-OHH. 2. H-c-OH + CH3-CH --OHH. OH + HOẠCH, H. 4....
4) Take a look at these structures of monosaccharides (3 pts) *CHOH CHOH CH,OH OH CH,OH SH HOM HO OH OH H H OH OH H . H OH GLUCOSE HOH GALACTOSE OH FRUCTOSE What is the molecular formula for the the following monosaccharides? a. glucose: C b. fructose: C c. galactose: C 5) A. Show the anomeric carbon. (1 pts) B. Draw B-D-Fructopyranose (2 pts) Fructose Isomers 6) Identify monosaccharide (M), disaccharide (D) or Polysaccharide (P) (3 pts) a....
12 13 4 5 6 24- Which of the following molecules have resonance structures? a) NBr. b)N, d) CO, c) 0 25-What is the molecular geometry if you have 4 single bonds around the central atom and no lone pairs? I a) Bent b) Tetrahedral c) trigonal pyramidal d) linear 26- Using the following Lewis structure and 3-dimensional structure of CH,OH answer the following questions? H 3- Hybridization of Oxygen b- Hybridization of Carbon CH-C-O bond angle d-HO-C bond angle...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
5. Write the IUPAC names/ draw
structures for the following: (10 points)
a through f please
5. Write the IUPAC names/ draw structures for the following: (10 points) a. 2,4,6-trinitotoluene(TNT) b. O2N NH2 c. 2,6-dichloroanisole d. CI CHO COOH .