2020_transcribed_NV_scibowl_finals

What is the name of this compound ? CH2-C=C-CH3 a) 3-butyl-1,3-hexadiene-5-yne b) 4-allyl-3-octen-6-yne c) 4-butynyl-3,5-hexadiene d) 5-vinyloct-5-en-2-yne e) 3-butynyl-1,3-hexadiene

1A Draw the structure of the following compounds: i) (S)-3-ethoxy-6-ethyloct-4-yne ii) (S)-6-methyl-3,3-dichlorocyclohex-1-ene

The reaction of 3-methylene-1-cyclohexene and HBr yields the four products shown in the attachment. Which two are formed at high temperatures and which two are formed at low temperatures? Why? Why is 1-bromo-3-methylenecyclohexane not formed?

Draw the structure of the following compounds. Use line-angle structural formula. 1-bromo-4-ethyl-5- methylcyclohexane 3,7-dimethyl-5-propylnonae 5-chloro-1- ethylspiro[2.5]octane 2-bromo-4- methylbicyclo[3.2.1]octane * 5-cyclobutyl-2-cyclopropyl- 6,8-diethyl-3,7,7- trimethyldecane *

Draw the molecular models of the compounds listed below: a) 5-methyl-(2E, 4Z)-2,4-octadiene b) 5-methyl-(2E, 4E)-2,4-octadiene c) 5-methyl-(2Z, 4Z)-2,4-octadiene

Start with the cyclohexene at the top of the page. You have a bank of structures below that you can use below. There are more structures in the bank than you need some of the structures in the bank are unnecessary, and some may belong in some of the unlabelled boxes. Which structure belongs in each of the numbered boxes? 1 4 LIAIH4 NaCN 1) SOCI₂ 2) NH₂ HBr 5 6 1) Mg 2) CO2 3) H3O+ CH3OH H* NBS hv LIAIH4 2 thi PCC NaOH NH₂ H* 2) LIAIH4 1) Na 2) 3 7 T

Solve it and also tell which rules of IUPAC are you using

3. The following alkenes can be prepared by dehydration of an appropriate alcohol. Show the structure of the alcohol in each case. If the alkene can arise from dehydration of more than one alcohol, show all possibilities. CH3CH2 C=CH2 CH3CH2 a) сH-с—снCH,CHз CH3 b) c) 3-hexene d) 1,3-butadiene

Directions: Decode the statement by finding the correct name of the structures below. Write the letter of the correct name on the blank. C - ethylcyclohexane E - 1-methyl-1-cyclopentene F- 2-pentyne H- cyclobutene I-2,2-dimethylpropane м- суclohexyne N- 2-hexene S- 2,4-dimethyl-2-pentene U - butane 1. 2. 3. CH3-C-CH3 CH3 CH-f=CH-CH-CH3 ČH3 5. 6. CH3-C=C-CH2-CH3 CH3-CH2-CH2-CH3 CH3-CH2-CH2-CH=CH-CH3 7. 8. 9. Activity 3. What's My Name? Directions: Study the structures below and give the correct name. CH2 CH3-CH2-CHz-CH3 CH2 CH C=CH CH3-CH=C-ç-CH-CH3 CH2 1. 2. 3. 6. 5. 4.

N,N-diethyl-m-toluamide (DEET) is the active ingredient in many insect repellent preparations. Following is one of the steps in its synthesis. In the box below draw the structure of the product of this reaction. H3C MgBr 1. CO2 2. H3O+ product • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Draw the Grignard reagent as a covalent magnesium bromide. 90-87 0 + 11 ? n [

Draw a structural formula for the major organic product of the following reaction: -CH=CH₂ + Br₂ ***** • Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If enantiomers are formed, just draw one. Sn [1 CH₂Cl₂ ChemDoodle Previous Next

Classify the following alkyl halide as primary, secondary, tertiary? and Why? CH₂Cl benzyl chloride cr chlorobenzene

What is the IUPAC name for the compound shown here? A) methylpentyne B) 2-methyl-3-pentyne C) 4-methyl-2-pentyne D) 3-methyl-1-butyne E) 2-methyl-3-butyne +

Please answer my question fast and be careful when you read the question

3- Answer the following questions based on your understanding of organic reactions: 1) 1-bromohexane 2) 3-bromo-3-methyl-pentane 4) 3-bromo-2-methylpentane 3) 1-bromo-2,2-dimethylbutane 5) 2-bromo-3-methylpentane Choose the alkyl halide(s) from the above list of C6H13Br isomers that meet each criterion below: a) the compound(s) that can exist as enantiomers b) the compound(s) that can exist as diastereomers c) the compound that gives the fastest SN2 with sodium methoxide d) the compound that is least reactive to sodium methoxide in methanol e) the compound(s) that give only one alkene during E2 f) the compound(s) give an E2 but no SN2 reaction with sodium methoxide in methanol g) the compound(s) that undergo SN1 reaction to give products with shifts h) the compound that gives the fastest SN1 reaction

The two alkenes below react with HI at different rates. CH3CH=CHCH3 and CH₂=CH₂ Draw the structural formula of the MAJOR product formed by the alkene having the HIGHER reaction rate. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. TAYY [ ] در ChemDoodle Ⓡ

N,N-diethyl-m-toluamide (DEET) is the active ingredient in many insect repellent preparations. Following is one of the steps in its synthesis. In the box below draw the structure of the product of this reaction. H3C MgBr 1. CO₂ 2. H₂O* product • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Draw the Grignard reagent as a covalent magnesium bromide.

2. Write the major products, if any, of each of the following reactions (please draw molecular structures, not just molecular formulas).

E2 S What is the correct IUPAC name for the following substance? CI (S)-1-chlorospiro[2.5]octane (S)-7-chlorospiro[2.5]octane (S)-2-chlorospiro[2.5]octane (R)-2-chlorospiro[2.5]octane (R)-7-chlorospiro[2.5]octane (R)-1-chlorospiro[2.5]octane

Draw a structural formula for the major product of the reaction shown.

Please be clear in your writing

Use the editor to format your answer Question 26 The following compound on flipping results in: A trans-1,4-dimethylcyclohexane (a,a) B trans-1,4-dimethylcyclohexane (e,e) cis-1,4-dimethylcyclohexane (e,e) D cis-1,4-dimethylcyclohexane (a,a) O 102 minutes remaining Type here to search

Give the IUPAC name for the following compound. To preview the image click here Br O 5-bromo-3,6-dimethyl-(3Z)-heptene O 5-bromo-3,6-dimethyl-(3E)-heptene O 3-bromo-2,5-dimethyl-(4Z)-heptene O 3-bromo-2,5-dimethyl-(4E)-heptene

What is the IUPAC name of the following molecule? s O 1-cyclohexyl-1,3,4-trimethyl-(1Z,3E)-1,3-hexadiene 6-cyclohexyl-3,4,6-trimethyl-(3E,5Z)-3,5-hexadiene O 6-cyclohexyl-3,4,6-trimethyl-(3Z,5E)-3,5-hexadiene 1-cyclohexyl-1,3,4-trimethyl-(1E,3Z)-1,3-hexadiene

N,N-diethyl-m-toluamide (DEET) is the active ingredient in many insect repellent preparations. Following is one of the steps in its synthesis. In the box below draw the structure of the product of this reaction. MgBr H3C 0 ▾ + 1. CO₂ 2. H3O+ • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Draw the Grignard reagent as a covalent magnesium bromide. n [ ]# product ChemDoodleⓇ 28

Draw a structural formula for the product formed upon hydroboration/oxidation of the alkene below. CHCH₂CH3 • Use wedge and hash bonds ONLY for rings. • Do not show stereochemistry in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer.

draw the structures below: 3-cyclopropyl-5-propylcyclopentene (4Z, 6E) - 3-bromo-4-ethyl-5-methyl -1,4,6 octatriene - trans-3-hexene cis-3-hexene 2-chloro-5-methyl-2-heptene

Draw these molecules: ✓/3-Isopropenyl-1.4-cyclohexadiene + (E)-1,2,4-hexatriene 6

Ⓒ Macmillan Learning Draw the structural formula of (3E,5Z)-5-ethyl-3,5 - nonadiene. An alternative name for this compound is (3E,5Z)-5-ethyInona - 3,5-diene, which follows the rules outlined in the 1993 IUPAC recommendations. मार

Draw a structural formula for the product formed upon hydroboration/oxidation of the alkene below. CH3 CH3 CH3CHCHCHCH=CH2 CH3 • Use wedge and hash bonds ONLY for rings. Do not show stereochemistry in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer. 0 + ? [F

The name of compound A in Figure 5 is 1-(butan-2-yl)-3-methylcyclohexane. Use this information to determine the IUPAC name of compound B. [Numbers are separated by commas and numbers and letters by hyphens Use lower case letters and do not use spaces.] *

Draw a structural formula for the substitution product of the reaction shown below. H/ ● (CH3)3C |YY Br ΔΟ H Na • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one stereoisomer of product is formed, draw both. Separate multiple products using the + sign from the drop-down menu. • Products that are initially formed as ions should be drawn in their neutral forms. SH acetone [F

Estimate the heat released when ethene(CH2=CH2) reacts with HBr to giveCH3CH2Br. Bond enthalpies areC-H : 412 kJ/mol; C-C : 348 kJ/mol;C=C : 612 kJ/mol; C-Br : 276 kJ/mol;Br-Br : 193 kJ/mol; H-Br : 366 kJ/mol. Choose the correct answer:1. 1036 kJ/mol2. 58 kJ/mol3. 424 kJ/mol4. 200 kJ/mol5. 470 kJ/mol

N,N-diethyl-m-toluamide (DEET) is the active ingredient in many insect repellent preparations. Following is one of the steps in its synthesis. In the box below draw the structure of the product of this reaction. H3C MgBr 1. CO2 2. H30* product • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Draw the Grignard reagent as a covalent magnesium bromide. P ору aste O O O- []# Previous Next Email Instructor Save and Exit