Draw three carbocations, each with the formula C9H19. Make one carbocation primary, one secondary and one...
Draw three carbocations, each with the formula C9H19. Make one carbocation primary, one secondary and one tertiary. Rank the relative stabilities of the three carbocations.
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Draw three carbocations, each with the formula
C9H19. Make one carbocation primary, one
secondary and one...
10 pts Question 6 Rank the following carbocations in order of increasing stability. Identify each of...
10 pts Question 6 Rank the following carbocations in order of increasing stability. Identify each of the carbocations as methyl, primary, secondary, or tertiary. CH, CH.CH -ён, сносе сна ін си, пенси, А es es | Select) [Select) < Select) [Select) Select) [Select] 4 Carbocation A: Select] Carbocation B: Select Carbocation C. Select Carbocation D: Select Carbocation E: Select] Carbocation : [Select]
for the general formula C5H12O draw the structures of three isomeric alcohols that illustrate primary secondary...
for the general formula C5H12O draw the structures of three isomeric alcohols that illustrate primary secondary and tertiary alcohol structures.
3. Carbocation Stability - classify the following carbocation as primary, secondary, or tertiary. highly unstable cations...
3. Carbocation Stability - classify the following carbocation as primary, secondary, or tertiary. highly unstable cations more electronegative sp2 orbital does not want to become cationic 4. Which of the following is more stable (lower in potential energy)? Explain your choice. وطرط 5. Rank the following carbocation in the order of increasing stability with 5 being the most stable carbocation. له مو و و او
1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms...
1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. 2. Rank the following free radical intermediates in order of increasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. CH2 bro ledo IV b III 10 112TV ] 21 3. 2,3-Dimethylbutane reacts with bromine in the presence of light to give a monobrominated product....
Draw the structural formula for a compound that contains a tertiary alcohol, a secondary alkyl halide,...
Draw the structural formula for a compound that contains a tertiary alcohol, a secondary alkyl halide, and primary, secondary and tertiary hydrogens. a. Indicate the number of beta-hydrogens relative the alkyl halide. b. Name the compound you just drew.
Draw structures with names of Primary, Secondary, Tertiary alcohols. Also draw the reaction with product as...
Draw structures with names of Primary, Secondary, Tertiary alcohols. Also draw the reaction with product as each kind of alcohol undergoes oxidation reaction. Draw the condensed structural formula.
Draw the structure of the secondary carbocation that could form in the hydrobromination of 2-brxene. CH_3CH_2CH_2CH=CHCH_3...
Draw the structure of the secondary carbocation that could form in the hydrobromination of 2-brxene. CH_3CH_2CH_2CH=CHCH_3 + HBr You do not have to consider stereochemistry. If two secondary carbocations are possible, draw both of them. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right Separate structures with + signs from the drop-down menu.
Draw one example each of a primary, a secondary and a tertiary amine as well as an ammonium 1. salt. Draw an alkene...
Draw one example each of a primary, a secondary and a tertiary amine as well as an ammonium 1. salt. Draw an alkene that can exist as a cis and a trans isomer. What are the two molecules to each 2. other? Draw fluorocyclohexane and show the intramolecular plane of symmetry. Then draw 1,2-cis- 3. difluorocyclohexane and 1,3-cis-difluorocyclohexane and indicate internal planes of symmetry if present.
VIII. (9 pts.) Each of the following carbocations will rearrange to form a different carbocation. Draw...
VIII. (9 pts.) Each of the following carbocations will rearrange to form a different carbocation. Draw the correct structure of each of the rearranged carbocations in the spaces provided and show how each rearranged cation will form using arrow formalism correctly. Feel free to add necessary detail to the each starting structure as need be. A. CHșCH,CH B. CH, C. (CH3)2CCHCH2CH3
4 (b) Some of the compounds below may carbocation. Please draw the structures of the carbocations...
4 (b) Some of the compounds below may carbocation. Please draw the structures of the carbocations that are formed. α undergo loss of the tooylane pop o form reaction" if no carbocation can be formed. If a carbocation consists of madiple res structure, draw two resonance structures. Also indicate which carbocation is the stable one. (20 points) NH2
10 pts Question 6 Rank the following carbocations in order of increasing stability. Identify each of the carbocations as methyl, primary, secondary, or tertiary. CH, CH.CH -ён, сносе сна ін си, пенси, А es es | Select) [Select) < Select) [Select) Select) [Select] 4 Carbocation A: Select] Carbocation B: Select Carbocation C. Select Carbocation D: Select Carbocation E: Select] Carbocation : [Select]
3. Carbocation Stability - classify the following carbocation as primary, secondary, or tertiary. highly unstable cations more electronegative sp2 orbital does not want to become cationic 4. Which of the following is more stable (lower in potential energy)? Explain your choice. وطرط 5. Rank the following carbocation in the order of increasing stability with 5 being the most stable carbocation. له مو و و او
1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. 2. Rank the following free radical intermediates in order of increasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. CH2 bro ledo IV b III 10 112TV ] 21 3. 2,3-Dimethylbutane reacts with bromine in the presence of light to give a monobrominated product....
Draw the structure of the secondary carbocation that could form in the hydrobromination of 2-brxene. CH_3CH_2CH_2CH=CHCH_3 + HBr You do not have to consider stereochemistry. If two secondary carbocations are possible, draw both of them. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right Separate structures with + signs from the drop-down menu.
Draw one example each of a primary, a secondary and a tertiary amine as well as an ammonium 1. salt. Draw an alkene that can exist as a cis and a trans isomer. What are the two molecules to each 2. other? Draw fluorocyclohexane and show the intramolecular plane of symmetry. Then draw 1,2-cis- 3. difluorocyclohexane and 1,3-cis-difluorocyclohexane and indicate internal planes of symmetry if present.
VIII. (9 pts.) Each of the following carbocations will rearrange to form a different carbocation. Draw the correct structure of each of the rearranged carbocations in the spaces provided and show how each rearranged cation will form using arrow formalism correctly. Feel free to add necessary detail to the each starting structure as need be. A. CHșCH,CH B. CH, C. (CH3)2CCHCH2CH3
4 (b) Some of the compounds below may carbocation. Please draw the structures of the carbocations that are formed. α undergo loss of the tooylane pop o form reaction" if no carbocation can be formed. If a carbocation consists of madiple res structure, draw two resonance structures. Also indicate which carbocation is the stable one. (20 points) NH2
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