Chrome File Edit View History Bookmarks Profiles Tab Window Help Aktiv X Aktiv Chemistry ?CO app.aktiv.com Sumdog Find Bongo avalla. Tarleton State Uni. Introduction to An. Kindle < Question 4 of 20 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. 7- 1- 3- 2- neo tert- di iso <> G6-ethylhept-2-yne- Google All Bookmarks Submit Q: Provide the correct systematic name for t IUPAC name for the compound shown he compound shown here. See a step by step Q: Provide the correct IUPAC name for the c Provide the correct IUPAC name for the c A: See a step by step answer Q:?Provide the correct IUPAC name for the CH3 CH3 Provide the correct IUPAC namer A: See a step by step answer Q: Provide the correct IUPAC name for the co Provide the correct IUPAC name for the co A: See a step by step Q: need help please! Provide the correct IUPA the correct IUPAC name for the compound for the compound shown here. CH_3-CH= Question 11 of 30 Provide the correct IUPA CH3 Provide the correct IUPAC name for th See a step by step answer appreciate the help. Provide the correct IUF Provide the correct IUPAC name for the cor IUPAC name for the compound shown here.
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Step 1: Identify the longest continuous carbon chain in the skeleton — this is six carbons, so the parent hydrocarbon is hexane. Show more…
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2. What is the IUPAC name of the compound on the right? A) 3,4-dimethyl-1-buten-4-ol B) 3-methyl-1-penten-5-ol C) 1,2-dimethyl-3-buten-1-ol D) 3-methyl-4-penten-2-ol E) 3-vinyl-2-butanol 3. What is the IUPAC name of the compound on the right? A) (R)-2-methyl-4-pentanol B) (S)-2-methyl-4-pentanol C) (R)-4-methyl-2-pentanol D) (S)-4-methyl-2-pentanol E) 2-hydroxy-4-methylpentane 4. What is the IUPAC name of the compound on the right? A) (E)-2-methyl-3-penten-2-ol B) (Z)-2-methyl-3-penten-2-ol C) (E)-1,1-dimethyl-2-buten-1-ol D) (Z)-4,4-dimethyl-2-buten-4-ol E) (E)-4-hydroxy-4-methyl-2-pentene 5. All of the compounds below have molecular weights very close to 60 g/mol. Which one has the highest boiling point? A) (CH3)2C=O B) HO-CH2-CH2-OH C) CH3CH2CHO D) CH3CH2CH2-OH E) CH3CH2C≡CH 6. All of the compounds below have molecular weights very close to 60 g/mol. Which one has the lowest boiling point? A) (CH3)2C=O B) HO-CH2-CH2-OH C) CH3CH2CHO D) CH3CH2CH2-OH E) CH3CH2C≡CH 7. Which one of the following alcohols cannot be easily oxidized with Jones reagent? A) 2-methyl-1-butanol B) 3-methyl-1-butanol C) 3-methyl-2-butanol D) 2-methyl-2-butanol E) 3,3-dimethyl-1-butanol
Madhur L.
a) Using the (E-Z) designation, give the IUPAC names for each of the following: a) CC H CH2CH2CH3 Br Cl b) CC CH3 CH2CH2 Cl I c) CC Br CH2CH2 Cl I d) CC CH2CH(CH3)3 CH3 H3C H 2. Predict the more stable alkene of each pair. a) 2-methyl-2-pentene or 2,3-dimethyl-2-butene b) Cis-3-hexene or trans-3-hexene c) 1-hexene or cis-3-hexene d) Trans-2-hexene or 2-methyl-2-pentene 3. List the alkenes that would be formed when each of the following alkyl halides is subjected to dehydrogenation with potassium ethoxide in ethanol and use Zaitsev's rule to predict the major product of each reaction: a) 2-bromo-3-methylbutane b) 2-bromo-2,3-dimethylbutane 4. The following dehydration follows an exception to Zaitsev rule. Predict the alkene structures of the major and minor products. C CH3 H3C CH3 O + C CH3 CH3 H3CH2C Br 75 0C (CH3)3COH 5. Write the missing reagents for the following transformations: a) CH3CH2OH 2HC CH2 + H2O B) 3HC C CH3 CH3 OH 3HC C CH3 CH2 + H2O C) OH + d) 3HC C C CH3 C C CH3 H3C H H C C H3C H H CH3 i) ii) 6. Write a structural formula for each of the following: a) E-2-pentene b) 3,3,3-tribromopropene c) Z-1-cyclopropyl-1-pentene d) 5-cyclobutyl-1-pentene e) E-4-methyl-4-hexen-1-yne 7. Outline a synthesis of cyclopentene from each of the following: a) Bromocyclopentane b) Cyclopentanol
Adi S.
A compound having a carbon atom attached to -H, -OH, -COOH, -OCOC2H5 groups. How many chiral carbons are in this compound? a. 1 b. 2 c. 3 d. 4 Question 2 Rank the following sets of substituents in order of priority (highest on the left) according to the Cahn-Ingold-Prelog sequence rules. a. 3 > 4 > 1 > 2 b. 2 > 4 > 1 > 3 c. 2 > 4 > 3 > 1 d. 4 > 2 > 1 > 3 Question 3 The IUPAC name of the below compound is a. 2-methyl-3-oxohex-4-enal. b. 3-oxo-2-methylhex-5-enal. c. 5-formylhex-2-en-3-one. d. 5-methyl-4-oxohex-2-en-5-al. Question 4 Lactic acid in which the methyl group, hydroxyl group, a carboxylic acid, and a hydrogen atom are attached to a central atom shows optical isomerism due to molecular geometry at the a. Oxygen of the hydroxyl group. b. Carbon atom of the carboxylic acid group. c. Carbon atom at the methyl group. d. Central carbon atom Question 5 Choose "A" and "B" for the below reaction. a. 2,3,3-trimethylpropanal and 2,3,3-trimethylbutanoic acid. b. 2,3,3-trimethylpentanal and 2,3,3-trimethylpentanoic acid. c. 2,3,3-trimethylbutanal and 2,3,3-trimethylbutanoic acid. d. 2,3,3-trimethylbutanal and 2,3,3-trimethylpentanoic acid. Question 6 Which of the following statements is not true for the biochemical method of resolution? a. One of the enantiomers is always destroyed. b. It is difficult to find specific microorganisms for racemic modification. c. It is one of the best methods, and we can get both enantiomers of a racemic mixture. d. Bacteria and molds are allowed to grow in a solution of a racemic modification. Question 7 Select a suitable reagent for the following reaction. a. P2S3 b. P2O5 c. P2O3 d. P2S5 Question 8 Which is the structure of R-limonene present in orange fruit? a. b. c. d. Question 9 Complete the following reaction. a. CH3(CH2)4CH2CH2SH. b. CH3(CH2)4SH. c. CH3(CH2)3SH d. CH3(CH2)4CH2SH. Question 10 Which of the following tautomeric forms is more stable? a. II. b. Both are unstable. c. Both are equally stable. d. I
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