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1. Name these compounds: *) HOSCH.HCH o cuddChuquichs b) Na - PCHCHICH " CH CH.CH)ÇUCH сн;...
1. Name these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) ne...
1. Name these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. CH,C=COH CH3C=CCH2OH 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOC12. a) CH;C=CCH,COH - снсесснRocнск b) CH3C=CCH_COH » CHỤC=CCHCNCH) ber these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. O...
2. Show the step(s) necessary to transform the compound on the left into the acid on...
2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,
3. Show the steps necessary to transform the acid on the left into the compound on...
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
3. Show the steps necessary to transform the acid on the left into the compound on...
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCI2 a) -CHCHOCH Р-снсн. Сон Н.С-СНСH,CoСНB Н-С-СНCH,COН несиси вусая, b) Н.С-СНСH,CоН нсснсн 2он Н,С-СНСH,CNСАНЯ CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 =easiest to hydrolyze, 4 hardest to hydrolyze. сHсн2нся. сновсм, CH2CH2CNHC&Hs CHоёсн, CH3CH2CCI N=CCH3
Q.4. Which of the following compounds is the strongest acid? a. CH b. CH.CH C. HỌC...
Q.4. Which of the following compounds is the strongest acid? a. CH b. CH.CH C. HỌC CHỊ d. HCECH Q.5. Which of the following is the strongest acid a. CH.CH b. CHÚNH с. СН,ОН d. CHF Q.6. Which of the following is easiest to deprotonate (removing a proton) ?! a CH b. CH.CH C. CH2=CH d. HCECH Q.7. Which of the following anions is the strongest base? a. CH,COO b. HO- C. NH" d. cr Q.8. Which set of curved...
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound...
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...
NAME 1. Give IUPAC names for the following compounds. CH, CH.CH a) HC=CCCH,CECH b) H.CCH,CHCECCH-CH-CH, CH,...
NAME 1. Give IUPAC names for the following compounds. CH, CH.CH a) HC=CCCH,CECH b) H.CCH,CHCECCH-CH-CH, CH, CH,CH, CH
- 6! Name the following compounds based on their structures (circle your answer) (6 pts tot сн. CH,CH.CH) a) eis-5-...
- 6! Name the following compounds based on their structures (circle your answer) (6 pts tot сн. CH,CH.CH) a) eis-5-methylhex-2-ene b) trans-5-methylhex-2-ene eis-2-methylhex-3-ene d) trans-2-methylhex-3-ene 2) A - H _ CH CHCH a) 3-methylbut-3-ene 62-ethylprop-1-ene c)2-methylbut-1-ene d) 2-ethylprop-2-ene hepta-2,6-diene b) hept-2,6-diene c) hepta-1,5-diene d) hept-1,5-diene сн. (H,сне H a) (E)-3-methylhex-3-ene b) (Z)-3-methylhex-3-ene (E)-4-methylhex-3-ene a) (2)-4-methylhex-3-ene CHÚCH). a 3-methylcyclopentene $) methylcyclopentene c) 5-methylcyclopentene CH3 a) 2,5-dimethylcyclohexa-1,5-diene 1,4-dimethylcyclohexa-1,3-diene c) 1,4-dimethylcyclohexa-4,6-diene Hoa
HELP What is the common UPAC name for the following compound? 1 нс b) 1-methyl-3-cyclohexene d)...
HELP
What is the common UPAC name for the following compound? 1 нс b) 1-methyl-3-cyclohexene d) 1-methyl-4-cyclohexene a) 5 methylcyclohexene c 4 methylcyclohexene Methylcyclohexene e) Which of the following is capable of exhibiting cis-trans isomerism? a) 1-pentene 2. b) 1-butene c) 2- pentene d) Cyclohexene e) Ethene What is the relationship between the following compounds: 3. Н,с a) Conformational isomers b) Constitutional isomers c) Configurational isomer d) Structural isomers e) Positional isomers Which of the following is the most stable...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
1. Name these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. CH,C=COH CH3C=CCH2OH 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOC12. a) CH;C=CCH,COH - снсесснRocнск b) CH3C=CCH_COH » CHỤC=CCHCNCH) ber these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. O...
2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCI2 a) -CHCHOCH Р-снсн. Сон Н.С-СНСH,CoСНB Н-С-СНCH,COН несиси вусая, b) Н.С-СНСH,CоН нсснсн 2он Н,С-СНСH,CNСАНЯ CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 =easiest to hydrolyze, 4 hardest to hydrolyze. сHсн2нся. сновсм, CH2CH2CNHC&Hs CHоёсн, CH3CH2CCI N=CCH3
Q.4. Which of the following compounds is the strongest acid? a. CH b. CH.CH C. HỌC CHỊ d. HCECH Q.5. Which of the following is the strongest acid a. CH.CH b. CHÚNH с. СН,ОН d. CHF Q.6. Which of the following is easiest to deprotonate (removing a proton) ?! a CH b. CH.CH C. CH2=CH d. HCECH Q.7. Which of the following anions is the strongest base? a. CH,COO b. HO- C. NH" d. cr Q.8. Which set of curved...
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...
NAME 1. Give IUPAC names for the following compounds. CH, CH.CH a) HC=CCCH,CECH b) H.CCH,CHCECCH-CH-CH, CH, CH,CH, CH
- 6! Name the following compounds based on their structures (circle your answer) (6 pts tot сн. CH,CH.CH) a) eis-5-methylhex-2-ene b) trans-5-methylhex-2-ene eis-2-methylhex-3-ene d) trans-2-methylhex-3-ene 2) A - H _ CH CHCH a) 3-methylbut-3-ene 62-ethylprop-1-ene c)2-methylbut-1-ene d) 2-ethylprop-2-ene hepta-2,6-diene b) hept-2,6-diene c) hepta-1,5-diene d) hept-1,5-diene сн. (H,сне H a) (E)-3-methylhex-3-ene b) (Z)-3-methylhex-3-ene (E)-4-methylhex-3-ene a) (2)-4-methylhex-3-ene CHÚCH). a 3-methylcyclopentene $) methylcyclopentene c) 5-methylcyclopentene CH3 a) 2,5-dimethylcyclohexa-1,5-diene 1,4-dimethylcyclohexa-1,3-diene c) 1,4-dimethylcyclohexa-4,6-diene Hoa
HELP
What is the common UPAC name for the following compound? 1 нс b) 1-methyl-3-cyclohexene d) 1-methyl-4-cyclohexene a) 5 methylcyclohexene c 4 methylcyclohexene Methylcyclohexene e) Which of the following is capable of exhibiting cis-trans isomerism? a) 1-pentene 2. b) 1-butene c) 2- pentene d) Cyclohexene e) Ethene What is the relationship between the following compounds: 3. Н,с a) Conformational isomers b) Constitutional isomers c) Configurational isomer d) Structural isomers e) Positional isomers Which of the following is the most stable...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
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