1. (5 pts) Provide products for the following reactions. Label them as chiral, achiral, meso, dl,...
need help with problem set e following reactions provide the missing products or reagents. (12 pts) 3. For the following Br AICI NO2 NH2 H2NNH2 кон heat Meo Cl2 FeCl3 Мео act as if they are two separate aromatic ring
2. (16 pts) Reactions Provide reagents, products or starting materials for the following reactions. Show stereochemistry when relevant (or loss thereof). If a reaction produces no significant products, write "NR". If you have a question about an abbreviation, just ask. NaBr OH 1. TsCI 2. Nal, DMF CI DMSO OH 1. PBrg NaCN 2. KOC(CH3)3 Ether LDA НОН THE NaH NaH PO Acetone Heat, water
1. Draw the (major) organic products of the following reactions: HNO3 H2SO4 HN (CH3)3CBr AlBr3 FeBr3 Br Sort the following molecules by their reactivity toward electrophilic aromatic substitution (1-most reactive, 4 2. least reactive): NH2 so,H Place either the letter A or C below the following compounds to indicate whether each of them are achiral (A) or chiral (C) 3. но Cl Determine the configuration (R or S) for each stereocenter in the following compounds: 4. Cl Cl NH2 но...
1. (4 pts) Provide products for the following reactions indicated below: NEOEU: HCI d. Citymalanato NEOEI il. HCL H-0 EIO OET + NaOH 100C Ph. i H H H HON NaBH CN O Br NH ј кон 2 HNNH, NH ex
all of them please QUESTION 1 1 points Save Answer Which of the following can have cis/trans isomers? Draw their isomers. CH3CH2CH=CH2 (CH3CH2)2CCHCH3 CH3CH2CH=CHCH3 CH2=CH2 QUESTION 2 1 points Save Answer Name the following compounds, with cis/trans nomenclature. trans-4-methyl-2-hexene trans-4-thyl-2-pentane O cis-4-thyl-2-pentane O cis-4-methyl-2-hexene QUESTION 3 1 points Save Answer Name the following compounds, with cis/trans nomenclature Br Br Otrsans-2,5-dibromo-3-hexene trans-1,4-dibromo-2-butane O cis-1,4-dibromo-2-butane cis 2,5-dibromo-3-hexene Click Save and Submit to see and submit Click Save All Answers to save all...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...