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please provide the structure and IUPAC name for each
7. Acetic acid Systematic name=ethanoic acid colorless...
Paragraph 7. Acetic acid Structure and IUPAC name for. • Oxalic acid (oh) • Malonic acid...
Paragraph 7. Acetic acid Structure and IUPAC name for. • Oxalic acid (oh) • Malonic acid (my) • Succinic acid (such) • Glutaric acid (good) . Adipic acid (apple) • Pimelic acid (pie)
Provide the systematic (IUPAC) name for the following structure. OH my OH Show transcribed image text
Provide the systematic (IUPAC) name for the following structure. OH my OH
What is the systematic IUPAC name for the following Organic compound? OH O a. 2-Ethyl-7-oxodecanoic acid...
What is the systematic IUPAC name for the following Organic compound? OH O a. 2-Ethyl-7-oxodecanoic acid O b. 2-Ethyl-1,7-dioxodecan-1-ol c. 3-Carboxy-8-oxoundecane d. 9-Ethyl-4-oxodecanoic acid e. 1-Hydroxydecan-1,7-dione f. 9-Ethyl-4-oxodecanal What is the correct IUPAC name for the following alkene? CH3 CH3CH2CHC=CH2 CH2CH3 a. 2-(sec-butyl)but-1-ene b. 3-isobutylbut-3-ene c. 4-ethyl-3-methylpent-4-ene d. 2-ethyl-3-methylpent-l-ene e. 3-methyl-4-ethylpent-4-ene f. 2-ethyl-3-methylhex-2-ene g. octene
please help me answer questions 2 through 6 thanks PILDI student titrated 0.180 g of an...
please help me answer questions 2 through 6
thanks
PILDI student titrated 0.180 g of an unknown acid with 0.10 M NaOH solution and the data set was obtained: mL of 0.IM NaOH pH mL of 0.1M NaOH pH 2.20 20 3.25 22 28 4.00 4.25 4.50 4.81 5.25 5.55 5.75 6.10 6.32 6.70 7.00 9.00 11.20 11.70 12.00 12.22 12.40 12.60 30 32 14 16 36 38 1. Prepare a titration curve using Microsoft Excel. See Appendix C for...
Please answer all questions 6) Identify the correct IUPAC systematic name for the structure below. who...
Please answer all questions
6) Identify the correct IUPAC systematic name for the structure below. who -CH H A) N-methyl-2-ethyl-5-methyloctanamide B) 6,N-dimethylnonane-3-carboxamide C) 5,N-dimethyl-2-ethyloctanamide D) 2-ethyl-5,N-dimethyloctanamide 7) Which of the following is the most reactive carboxylic acid derivative? A) ester B) anhydride C) nitrile D) acid chloride E) amide 8) Identify the carboxylic acid derivative/s in the structure of Lactimidomycin. HN OH O A) Ester B) Anhydride C) Nitrile D) Imine 9) Arrange the carboxylic acid derivatives below in order...
7. The IUPAC name for the followe d in the OH controls a) 3-chloro-2-methylcyclohexanol 5-chloro-2-methylcyclohexanol 2-methyl-3-chlorocyclohexanol...
7. The IUPAC name for the followe d in the OH controls a) 3-chloro-2-methylcyclohexanol 5-chloro-2-methylcyclohexanol 2-methyl-3-chlorocyclohexanol d) 2-methyl-5 chlorocyclohexanol e) 1-chloro-4-methylcyclohexanol Which of the following cannot be an electrophile? a) H b) CH2-CH; c) 'NO ) BF; d) Fee ased on the following enery diagram, which compound is formed slowly Reaction ) B from A c) Cfrom B d) from C a) A from B b 10. Which of the following has the highest priority? -0-H -CH=CHCH -CH=NCH -SC-CH; 11....
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Paragraph 7. Acetic acid Structure and IUPAC name for. • Oxalic acid (oh) • Malonic acid (my) • Succinic acid (such) • Glutaric acid (good) . Adipic acid (apple) • Pimelic acid (pie)
Provide the systematic (IUPAC) name for the following structure. OH my OH
What is the systematic IUPAC name for the following Organic compound? OH O a. 2-Ethyl-7-oxodecanoic acid O b. 2-Ethyl-1,7-dioxodecan-1-ol c. 3-Carboxy-8-oxoundecane d. 9-Ethyl-4-oxodecanoic acid e. 1-Hydroxydecan-1,7-dione f. 9-Ethyl-4-oxodecanal What is the correct IUPAC name for the following alkene? CH3 CH3CH2CHC=CH2 CH2CH3 a. 2-(sec-butyl)but-1-ene b. 3-isobutylbut-3-ene c. 4-ethyl-3-methylpent-4-ene d. 2-ethyl-3-methylpent-l-ene e. 3-methyl-4-ethylpent-4-ene f. 2-ethyl-3-methylhex-2-ene g. octene
please help me answer questions 2 through 6
thanks
PILDI student titrated 0.180 g of an unknown acid with 0.10 M NaOH solution and the data set was obtained: mL of 0.IM NaOH pH mL of 0.1M NaOH pH 2.20 20 3.25 22 28 4.00 4.25 4.50 4.81 5.25 5.55 5.75 6.10 6.32 6.70 7.00 9.00 11.20 11.70 12.00 12.22 12.40 12.60 30 32 14 16 36 38 1. Prepare a titration curve using Microsoft Excel. See Appendix C for...
Please answer all questions
6) Identify the correct IUPAC systematic name for the structure below. who -CH H A) N-methyl-2-ethyl-5-methyloctanamide B) 6,N-dimethylnonane-3-carboxamide C) 5,N-dimethyl-2-ethyloctanamide D) 2-ethyl-5,N-dimethyloctanamide 7) Which of the following is the most reactive carboxylic acid derivative? A) ester B) anhydride C) nitrile D) acid chloride E) amide 8) Identify the carboxylic acid derivative/s in the structure of Lactimidomycin. HN OH O A) Ester B) Anhydride C) Nitrile D) Imine 9) Arrange the carboxylic acid derivatives below in order...
7. The IUPAC name for the followe d in the OH controls a) 3-chloro-2-methylcyclohexanol 5-chloro-2-methylcyclohexanol 2-methyl-3-chlorocyclohexanol d) 2-methyl-5 chlorocyclohexanol e) 1-chloro-4-methylcyclohexanol Which of the following cannot be an electrophile? a) H b) CH2-CH; c) 'NO ) BF; d) Fee ased on the following enery diagram, which compound is formed slowly Reaction ) B from A c) Cfrom B d) from C a) A from B b 10. Which of the following has the highest priority? -0-H -CH=CHCH -CH=NCH -SC-CH; 11....
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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