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Draw the structural formula for each of the following. (16 pts, 4 pts each) Draw a structural formula for each of th...
3. (16 pts, 4 pts each) Draw a structural formula for each of the following compounds...
3. (16 pts, 4 pts each) Draw a structural formula for each of the following compounds that have a complex substituent. First interpret the name of the parent compound, then interpret the name of the substituent given in parentheses. By convention, the carbon atom of the substituent attached to the parent chain or ring is designated a. 4-(1,1-dimethylethyl)-4-octanol b. 3-chloro-2-(1-hydroxyethyl)-6-nitrophenol c. 3-2-fluoro-2.propenyl)-5-hepten-2-one d. 4-(1-methylethyl)-5-methyl-3-hexenal
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH)...
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH) i 0 CO,H CH, OH Font Font COOH CH,_ch, bi-ch, bi-CH, CN CH OH CHO Font соон NO 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-Amino-2-methylbutanol b. 4-Hexynol C. 3-Methoxycycloheptanecarboxylic acid d. 2-Phenylethanol e. 3-Hydroxycyclopentanecarboxamide f. 4-Bromobenzaldehyde Font g. 6-Bromohexanoic acid h. 2, 3, 4-Hexanetriol L1-Decanthi 3. (16 pts, 4 pts each) Draw a structural formula for...
(4 pts) Ephedrine, shown below, is a potent dilator of air passages. The naturally occurring stereoisomer is levo...
(4 pts) Ephedrine, shown below, is a potent dilator of air passages. The naturally occurring stereoisomer is levorotatory with an (a) of -41º. Assign R or S to each stereocenter. How many stereoisomers of Ephedrine are possible? H NHCH3 HOW TO 4 stereo isomers - (12 pts) Are the following pairs of drawings representing identical, enantiomeric or diastereomeric relationships? 9 R HC a Hobo oh Diastereomeric HCOH C- Id CH pe H Identical Hace Diastereomeria $ (16 pts, 4 pts...
draw a structure for the following compounds compounds: Draw a structure for the following 14-(1,1-Dimethylethyl) –...
draw a structure for the following compounds
compounds: Draw a structure for the following 14-(1,1-Dimethylethyl) – 4-octanal <3 - Chloro-2-(4-hydroxyethyl) -6- nitrophenol ③ 3-(2-Fluoro-2-ProPenyl)-5-hepten-2-one 6 4-(1-methylethyl)-5-methyl-3-hexanal
Give the IUPAC names for each of the following: Draw a structural formula for each of...
Give the IUPAC names for each of the following: Draw a structural formula for each of the following: i) 4-ethoxy octane ii) cis-4-tert-butyl cyclohexanol iii) (R)-5-hexen-3-ol iv) 2-chloro-2, 3, 5-heptatriol
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol...
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol c. 5,5-diethyl-1-heptanol d. 2-ethyl-4-isopropylcyclohexanol e. 4-ethylphenol f. 2-nitrophenol g. cyclopropyl methyl ether h. isopropyl propyl ether 8.2 Give the product for the dehydration of each of the following alcohols. CH-CH2-CH3 a. ОН b. ОН C. OH d. 8.3 What product would result from the oxidation of each of the following alcohols? Write the chemical equations. a. 2-butanol b. 2-methyl-2-pentanol c. cyclohexanol d. 3-ethylcyclopentanol Name...
3. 12 pts. Draw the structural formula for the following amines and amides: a. Diethylamine &n
3. 12 pts. Draw the structural formula for the following amines and amides: a. Diethylamine d. 2-amino-4-hydroxy heptane b. 3-methyl aniline e. N-methyl-1-amino pentane c. 3-amino-3-methyl-2-hexanol f. propanamide 4. 3 pts. Write out the chemical reaction of ethyl amine with HCl. Use the structural formula for the reactant and product. Name the product. 5. 3 pts. Write out the structures and complete the reaction for: 1-amino pentane + HCl
2. Draw the condensed structural condensed formula and skeletal structure of each of the following alkyl...
2. Draw the condensed structural condensed formula and skeletal structure of each of the following alkyl groups. These names and formulas must be momorded. You can use to designate the parent chain to which each group is attached Methyl: Propyt: Isopropyt sec-Buty: Isobutyl: tert-Butyl: 3. Determine the IUPAC name of each of the following alkanes. CH,CH, CH,CHCH,CH,CHCH.CHCH.CH C(CH,
1) Draw the structural formula (line angle formula) given the following condensed formulas (6 pts) a)...
1) Draw the structural formula (line angle formula) given the following condensed formulas (6 pts) a) CH.CH-CH:CH OH b) CH,COOH c) CH.CH OCH 2) Draw the structural formula (line angle formula) given the following space filling models (Blue atoms are nitrogens and has 3 bonds; red atoms are oxygen and has 2 bonds) (6 pts.) b)
1.(a) (2pts.) Draw the structural formula for each amine. (b) provide the IUPAC name the structure...
1.(a) (2pts.) Draw the structural formula for each amine. (b) provide the IUPAC name the structure below 4-aminobutanal (R)-2-butanamine 2. (6 pts.) Consider the Grignard reaction shown below which forms a C-C bond via an Aw step. In box A, draw the structure of the nucleophile involved in the A step and highlight the nucleophilic atom. In box B, draw the structure of the electrophile involved in the Aw" step and circle the electrophilic atom. In box C, draw the...
3. (16 pts, 4 pts each) Draw a structural formula for each of the following compounds that have a complex substituent. First interpret the name of the parent compound, then interpret the name of the substituent given in parentheses. By convention, the carbon atom of the substituent attached to the parent chain or ring is designated a. 4-(1,1-dimethylethyl)-4-octanol b. 3-chloro-2-(1-hydroxyethyl)-6-nitrophenol c. 3-2-fluoro-2.propenyl)-5-hepten-2-one d. 4-(1-methylethyl)-5-methyl-3-hexenal
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH) i 0 CO,H CH, OH Font Font COOH CH,_ch, bi-ch, bi-CH, CN CH OH CHO Font соон NO 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-Amino-2-methylbutanol b. 4-Hexynol C. 3-Methoxycycloheptanecarboxylic acid d. 2-Phenylethanol e. 3-Hydroxycyclopentanecarboxamide f. 4-Bromobenzaldehyde Font g. 6-Bromohexanoic acid h. 2, 3, 4-Hexanetriol L1-Decanthi 3. (16 pts, 4 pts each) Draw a structural formula for...
(4 pts) Ephedrine, shown below, is a potent dilator of air passages. The naturally occurring stereoisomer is levorotatory with an (a) of -41º. Assign R or S to each stereocenter. How many stereoisomers of Ephedrine are possible? H NHCH3 HOW TO 4 stereo isomers - (12 pts) Are the following pairs of drawings representing identical, enantiomeric or diastereomeric relationships? 9 R HC a Hobo oh Diastereomeric HCOH C- Id CH pe H Identical Hace Diastereomeria $ (16 pts, 4 pts...
draw a structure for the following compounds
compounds: Draw a structure for the following 14-(1,1-Dimethylethyl) – 4-octanal <3 - Chloro-2-(4-hydroxyethyl) -6- nitrophenol ③ 3-(2-Fluoro-2-ProPenyl)-5-hepten-2-one 6 4-(1-methylethyl)-5-methyl-3-hexanal
Give the IUPAC names for each of the following: Draw a structural formula for each of the following: i) 4-ethoxy octane ii) cis-4-tert-butyl cyclohexanol iii) (R)-5-hexen-3-ol iv) 2-chloro-2, 3, 5-heptatriol
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol c. 5,5-diethyl-1-heptanol d. 2-ethyl-4-isopropylcyclohexanol e. 4-ethylphenol f. 2-nitrophenol g. cyclopropyl methyl ether h. isopropyl propyl ether 8.2 Give the product for the dehydration of each of the following alcohols. CH-CH2-CH3 a. ОН b. ОН C. OH d. 8.3 What product would result from the oxidation of each of the following alcohols? Write the chemical equations. a. 2-butanol b. 2-methyl-2-pentanol c. cyclohexanol d. 3-ethylcyclopentanol Name...
2. Draw the condensed structural condensed formula and skeletal structure of each of the following alkyl groups. These names and formulas must be momorded. You can use to designate the parent chain to which each group is attached Methyl: Propyt: Isopropyt sec-Buty: Isobutyl: tert-Butyl: 3. Determine the IUPAC name of each of the following alkanes. CH,CH, CH,CHCH,CH,CHCH.CHCH.CH C(CH,
1) Draw the structural formula (line angle formula) given the following condensed formulas (6 pts) a) CH.CH-CH:CH OH b) CH,COOH c) CH.CH OCH 2) Draw the structural formula (line angle formula) given the following space filling models (Blue atoms are nitrogens and has 3 bonds; red atoms are oxygen and has 2 bonds) (6 pts.) b)
1.(a) (2pts.) Draw the structural formula for each amine. (b) provide the IUPAC name the structure below 4-aminobutanal (R)-2-butanamine 2. (6 pts.) Consider the Grignard reaction shown below which forms a C-C bond via an Aw step. In box A, draw the structure of the nucleophile involved in the A step and highlight the nucleophilic atom. In box B, draw the structure of the electrophile involved in the Aw" step and circle the electrophilic atom. In box C, draw the...
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