b. cyclohexstant when the following B.23 Draw the structures of the chief product the formed are...
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What is the product of this bromination reaction? H2C-CH=CH-CH2-CH2-CH3 + Br2 3. What is the product of this oxidation reaction? OH H3C-CH-CH-CHg 10 Сн, 4. Consider the esterification reaction reaction below: H, SO H3C-CH2-CH2-CH2-C-OH + H2C-CH2-OH What organic compound is the reactant on the left? What organic compound is the reactant on the right? Draw the product of the reaction. What type of organic compound...
Draw the organic product formed in each reaction. Draw the organic product formed in each reaction 2) NNH, (2 Equiv) -CH=CH- 1) CH3-CH2-c=c 2)H,00 HCI (1 Equiv) - CC-H 1) Choc 2) H30 1) NaH =CH-CH-CH, D.O нсас 8 | H (deuterated water) d CH3CH2CH2CH OH нсис " HCE C H.CH 2) сн.
ES Click the "draw structure" button to launch the drawing utility. Draw the principal organic product for the following reaction. 49 СН3СН-СН-СН-СН-СН-СН2ОН PCC — CH2C12 draw structure... What is the product of the reaction shown below? C CIIZO Nat СНЊОН CH, points А) CHOCH,C(CH), ОН (3 02033 B) HOCH-C(CH), OH C) HOCH-C(CH3) ОСН, D) CH3OCH_C(CH3)2 Multiple Choice
Part A Draw the structure of the product that is formed when the compound shown below is treated with the following reagents: 1) BHZ. THF: 2) H2O2. HO Interactive 3D display mode CH3 ОН Part A Draw the product formed when the compound shown below undergoes reaction with HCl in MeOH. Interactive 3D display mode CH3 H,C
12.18 Draw the condensed structural formula of the aldehyde or ketone formed when each of the following alcohols is oxidized [O] (if no reaction, write none): CH3 a. CH3-CH-CH2-CH2-OH ОН b. CH3-CH2-C- CH3 CH3 ) ОН c. CH3-CH2-CH-CH2-CH3 d. OH
4. Draw the structures of the compounds formed in the following synthetic schemes. Br2 (CH3)2CHCH2CH3 UV NaOEt HBr C ROOR 1. Br2 E KOTBU ETOH 2. NaNH2(xs) 3. Нао light a. OH CHCH3 TsCl -сHа HBr B ROOR Кови A На C NaCECH 1. BH E 2. H2O2 NaOH F base Lindlars catalyst b. Br NaOMe HBr A ROOR 1. Br2 с 2. NANH2(xs) 3. H2O KOtBu В (CH3)2CCH2CH3 D MeOH с. Br2 NaOMe HBr c NaC CHD На (CH3)3CH...
12.36 Draw Fischer projections for each of the following dash-wedge structures: a. CHO b. CHO C. CHO с но : Br CH OH Ho : н СН,ОН н : ОН СН,ОН
[References) Choose the structures of the products that are formed when each of the following ethers is hydrolyzed: -CH2-O-CH2- (Select all that apply.) -CH2-CH2-OH CH2-OH -CH2-OH -CH2-CH2-OH OH OH O-CH2-CH3 CH3-CH2-CH2-CH-CH2-CH3 (Select all that apply.) D HO-CH2-CH3 OH CH3-CH2-CH2-CH-CH3 ОН CH3-CH2-CH2-CH-CH2-CH3 CHO-CH2-CH2-CH3 O CHE HO-CH-CH OH CH3-CH2-CH-CH2-CH3
1. Draw the product(s) of the following reactions. Include stereochemistry when relevant. If stereoisomers are formed then draw out and label the relationship between your structures. Ph-N3 40°C HN-NH2 SACOMe 150 °C d. CO2CH3 210 °C нсОСН3 In hv ZI 160 °C OBn 85 °C OBn OBno= o 1 equiv. CI K2CO3 heat PhCH N= H 1. LDA (1 equiv.) P 2. Ph Ph 3. aqueous work-up heat EtOH NaOEt 2. Draw the mechanism for the following transformations. I Н...
Draw both resonance structures of the product formed when the following starting material is treated with LDA in THF solution at -78°C. draw structure ... draw structure ... (Negative charge on carbon) (Negative charge on nitrogen)