2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе mos...
Select all the pairs that are cis-trans isomers. Н Н-с— сн, н and H;C HаС — сн Н Нс Н.с—сн, н and H. Н Нас— сн H. Нс CH3 н CH3 CH-CH CH-CH and Н Н н.с н Н,с—сн Н,с—сн, H. and CH, Н,с H. H. semsof use contact u about us privacy policy help careers F7 FS F6 F3 & 8 4 { Н G
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с Сн, Н CH,CH нс H 15. (3 pts each) Give the product(s) for the following reactions, and name all reactants and products. CH, он ОН н,с + нэс- сн - сн 3 нус. NH2 ОН Hн ІІ ОН + н-с-с-о-н НО P н Н ОН
alexis Naming Hydrocarbons Compatibility Mode Review View Help Mailings References Layout 1 I 2 3 Naming Worksheet - Hydrocarbons Name: Name of compound H,с- CH CH сH, 1 CH2 CH3 Нас Сн CH 2. Нас нас Methylcyclohexane 3. CHз I Br 4. Hас-нс -сн>-CH-CH, Н.с -сн CH3 -CHз 5. Н.с — сн — с CH3 H3C-CH-CHECH-CH2 CH3 6 но 7. Нс с сн 8 DFocus он DELL O co 6 1 Нас - CH2 CH3 C-CH3 CH3 H3C-CH2-CHECH-CH2 CH3 5....
6. Give IUPAC names for the following compounds b) а) CH,-CH,-CH-сH-с-сн, -сн, -сн, сн, CHCH X Cн, CH,-CHCH) - CH-сH, -CH Н CH CH С-с н нн CH2 CH CH(CH) Н.С - СH-СН-СН-СH н Н н сн, сн, CH С -с CH h) CH, -CH, -сH CH3 i)
just want to double check my answers Shit Alt 4. (4 pts.) The mechanism for the formation of an ester is comprised of the following steps. Identify each of the elementary steps and draw curved arrows to show movement of electrons. Be sure to draw in necessary nonbonding electron pairs +HSO, -S0,H OH нс OH н,с :он H Pro Гон H,C-C AU ie pddihon он 5.advs Н,с. "сн, 2cei он он H Н,с -он OH Нс H,C Palon Thek :0-CHs...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
having trouble with R and S configuration, can someone help out with this sheet? 17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
CНз С. CH 1 mol. Нас" ОН CH3 О НО—Р—ОН ОН ff Н2 Н2 С. ,HаС Но. 1 mol. CH2 Н,С. HО—Р—ОН ОН Оf+ О—-
1. Draw the following compounds. Each question is out of two marks. Drawing Name 2-phenyl hexanal 2-ethyl octan-1,2,7-triol para-chlorophenol cis-pent-3-en-2-ol 1,3-diphenylpropan-2-one ethyl butanoate 4-hydroxy-4-propyl hept-2,5-diene-1-amide N-pentyl-2,3-difluoro butanamide 2. Name the following compounds. Each question is out of two marks. Drawing Name CH3 CH Н.С Он Н. Н. Н.С Н. Н Н.С Н Н с Н CH CH НАС Н.С. CH2 Н.С. Н сн. HC H2 CH, CH Он Н.С CH, Н С. Н H C Н.С Н. На CH Н.С...
Reaction C Select Rings Draw More Erase С Н N Na NaOH Н2 с, CНз Нас CHз Reaction D Select Rings Erase Draw More Li C CНз .CH LIOH CH3 НО CHз IC Draw all of the products formed in each reaction. Include all hydrogen atoms. Reaction A Select Rings Draw More Erase С Н CНз CHз heat H-N НО .CH Hас CH3 Reaction B Erase Rings More Draw Select Cl O H Н2 НСІ CH3 Нас .CH НаС. CH3...