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24 - Write the IUPAC name of the following skeletal structures. Specify (R), (5), (E), (z)...
09 - Write the IUPAC name of the following skeletal structures. Specify R, S, E, Z...
09 - Write the IUPAC name of the following skeletal structures. Specify R, S, E, Z while naming. Q10 - Draw the skeletal structure of the following molecule. A) 3-Methyl-3-phenylbutanal B) 4-Hydroxy-4-methyl-2-pentanone C) Formaldehyde D) Benzaldehyde
5. Draw structure for the names and write the IUPAC name for the structures to points)...
5. Draw structure for the names and write the IUPAC name for the structures to points) Tho priority of functional groups for naming is: alkane < alkyl halide <ether <alkene alkyne < amine < alcohol ketone <aldehyde <carboxylic acid NH2 a. 3-chloro-4,4-dimethyl-1-nonen-6-yne d. (3E, 5Z)-2,6-Dimethyl-1,3,5,7-octatetraene
Determine the (E) and (Z) configuration and give the IUPAC name for the following alkenes. Verify...
Determine the (E) and (Z) configuration and give the IUPAC
name for the following alkenes.
Verify answers if correct.
2. Determine the (E) and (Z) configuration and give the IUPAC name for the following alkenes. trans-but 2-ene cis-but-2-ene (2)-3-bromo-one (E)-but-2-ene (2)-but-2-ene. (E)-1-bromo-2- methyl-1- cyclohexene (E)-3-jodo-4-methyl- 3-hexene (2)-3,4-dimethyl-2-hexene
Q1 - Write the IUPAC name of the following molecule including stereochemistry, (R) or (S), (2)...
Q1 - Write the IUPAC name of the following molecule including stereochemistry, (R) or (S), (2) or (E) where appropriate. 2 - Draw the skeletal structure for each of the following compounds. 4-cyclopentylbut-2-yne (Z)-4-fluoro-5-methylhept-4-en-2-yne 3- Which of the following alkynes is more stable?
1. Write IUPAC name of the following compounds? Include their stereochemistry (E, Z or cis-trans) in...
1. Write IUPAC name of the following compounds? Include their stereochemistry (E, Z or cis-trans) in their names.
Provide an IUPAC name for each of rhe following compounds shown. Specify (E)/(Z) stereochemistry, if relevant, for stra...
Provide an IUPAC name for each of rhe following compounds shown.
Specify (E)/(Z) stereochemistry, if relevant, for straight
chain alkenes only. Pay attention to commas, dashes, etc
CH3 CHCI CI C=C C H. HH н CHCH(CH3)2 CH3 Br CH3 c=c H2C- CH2 H CH3 CHCI C=C
a 5). Write the products for the jonization of the following carboxylic acids in 1. CH3-CHz-6-0H+H0...
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....
Name the following compounds. Don't forget to specify stercochemistry when appropriate 2. Draw the structures of...
Name the following compounds. Don't forget to specify stercochemistry when appropriate 2. Draw the structures of cis-2-ethylhexa-1,4-diene E-2,4-dimethylhexa-1,4-diene 3. Assign E or Z configuration to the following alkenes. (Circle highest priority groups) Br сн Вr сH,сн,Br NH2CH CH2CHCH CH,OH NH2 CH2CH2Br NEC Which of the following compounds that can exist as a mixture of stereoisomers? Draw each b. 1-chloro-2-methylbut-2-ene 4. a. 1-chloropropene c. 1,1-dichloroethene 5. Calculate the degree of unsaturation for codeine, CisHaiNO,. Show your work. 6. Rank the following...
Provide the appropriate IUPAC name for the following structure. Include E or Z notation. Br 5...
Provide the appropriate IUPAC name for the following structure.
Include E or Z notation.
Br 5 ク
please answer d e f g For each of the following structures: (a) Give the IUPAC...
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3- (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose...
09 - Write the IUPAC name of the following skeletal structures. Specify R, S, E, Z while naming. Q10 - Draw the skeletal structure of the following molecule. A) 3-Methyl-3-phenylbutanal B) 4-Hydroxy-4-methyl-2-pentanone C) Formaldehyde D) Benzaldehyde
5. Draw structure for the names and write the IUPAC name for the structures to points) Tho priority of functional groups for naming is: alkane < alkyl halide <ether <alkene alkyne < amine < alcohol ketone <aldehyde <carboxylic acid NH2 a. 3-chloro-4,4-dimethyl-1-nonen-6-yne d. (3E, 5Z)-2,6-Dimethyl-1,3,5,7-octatetraene
Determine the (E) and (Z) configuration and give the IUPAC
name for the following alkenes.
Verify answers if correct.
2. Determine the (E) and (Z) configuration and give the IUPAC name for the following alkenes. trans-but 2-ene cis-but-2-ene (2)-3-bromo-one (E)-but-2-ene (2)-but-2-ene. (E)-1-bromo-2- methyl-1- cyclohexene (E)-3-jodo-4-methyl- 3-hexene (2)-3,4-dimethyl-2-hexene
Q1 - Write the IUPAC name of the following molecule including stereochemistry, (R) or (S), (2) or (E) where appropriate. 2 - Draw the skeletal structure for each of the following compounds. 4-cyclopentylbut-2-yne (Z)-4-fluoro-5-methylhept-4-en-2-yne 3- Which of the following alkynes is more stable?
1. Write IUPAC name of the following compounds? Include their stereochemistry (E, Z or cis-trans) in their names.
Provide an IUPAC name for each of rhe following compounds shown.
Specify (E)/(Z) stereochemistry, if relevant, for straight
chain alkenes only. Pay attention to commas, dashes, etc
CH3 CHCI CI C=C C H. HH н CHCH(CH3)2 CH3 Br CH3 c=c H2C- CH2 H CH3 CHCI C=C
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....
Name the following compounds. Don't forget to specify stercochemistry when appropriate 2. Draw the structures of cis-2-ethylhexa-1,4-diene E-2,4-dimethylhexa-1,4-diene 3. Assign E or Z configuration to the following alkenes. (Circle highest priority groups) Br сн Вr сH,сн,Br NH2CH CH2CHCH CH,OH NH2 CH2CH2Br NEC Which of the following compounds that can exist as a mixture of stereoisomers? Draw each b. 1-chloro-2-methylbut-2-ene 4. a. 1-chloropropene c. 1,1-dichloroethene 5. Calculate the degree of unsaturation for codeine, CisHaiNO,. Show your work. 6. Rank the following...
Provide the appropriate IUPAC name for the following structure.
Include E or Z notation.
Br 5 ク
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3- (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose...
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