Homework Answers
1.Name of the shown alkene : Since Higher priority groups are on same side , so it is a Z-Alkene.
It is numbered from double bond , with sp2 carbons numbered as 1 and 2 in sequence.
Z - 1,2,4-trimethylcyclopentene
2. Given compound reacts with Ozone to form ozonide (ozone is inserted between carbons connecting double bond), which followed by reductive work up by Zn-Acetic acid gives 2,5-diketone.
It is example of Ozonolysis of a Alkene.
Add Answer to:
name the following alkene. (include E/Z designations in your names
if appropriate. Omit customary italics.)
Draw...
Name the following alkene. ball & stick + labels (Include E/Z designations in your names if...
Name the following alkene. ball & stick + labels (Include E/Z designations in your names if appropriate. Omit customary italics.) 2,4-dimethyl-3-heptene
Name all of the branched alkene isomers, CH12, that contain 2 methyl branches. pt Include E/Z...
Name all of the branched alkene isomers, CH12, that contain 2 methyl branches. pt Include E/Z designations in your names if appropriate. Omit customary italics. If there are fewer than 4 possible compounds, leave the appropriate number of fields blank. Isomer 1: 2,3,-dimethyl-2-butene Isomer 2: 2,3-dimethyl-1-butene Isomer 3: 3,3-dimethyl-1-butene Isomer 4: pt pt pt pt pt
Draw the product(s) of the reaction of the alkene below with O3, followed by Zn in...
Draw the product(s) of the reaction of the alkene below with O3, followed by Zn in acetic acid.
Name the following including the R/S, E/Z designations. 4. CH3 CH3 Hас Draw the complete mechanism...
Name the following including the R/S, E/Z designations. 4. CH3 CH3 Hас Draw the complete mechanism for the following E2 reaction, showing all arrows, intermediates, all products, and label the major product. 5. CH3 о CH3 Hас C. H2 CH3
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick labels ball & stick labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. • Use the wedge/hash bond tools to indicate stereochemistry where...
1) Provide the proper IUPAC name for the alkene shown below. CH2=CHCH2CH2CH2CH3 2) Provide the proper...
1) Provide the proper IUPAC name for the alkene shown below. CH2=CHCH2CH2CH2CH3 2) Provide the proper IUPAC name for the alkene shown below. 3) Draw an acceptable structure for 4-ethylhept-1-ene. 4) Provide an acceptable name for (CH3)2CHCH-C(CH3)CH2CH3. 5) Provide an acceptable name for (CH3CH2)2CHCH2CH-CH2. 6) Name the compound shown below. 7) Provide the proper IUPAC name for the alkene shown below. 8) Provide the proper IUPAC name for the alkene shown below. 9) Draw an acceptable structure for 4-phenylbut-l-ene. 10)...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
8.1) 8.5) Give the appropriate IUPAC name for the following structural formula of a halogenated compound....
8.1)
8.5)
Give the appropriate IUPAC name for the following structural formula of a halogenated compound. CH3 CI Нас (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis/trans designations only to represent stereochemistry for cyclic compounds. It is not necessary to use italics in writing compound names.) Name: There are five cycloalkanes with the molecular formula C5H10. When treated with chlorine at 300°C, isomer A gives one monochlorination product. Under the same conditions, isomer B...
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S l...
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.,...
Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate. draw the...
Draw the products of the following reactions, indicating both
regiochemistry and stereochemistry when appropriate.
draw the organic product(s) expected when this compound
undergoes the Simmons-Smith reaction.
Draw the product of the reaction below.
Reaction of 3-methyl-1-butene with
CH3OH in the presence of H2SO4
catalyst yields 2-methoxy-2-methylbutane by a
mechanism analogous to that of acid-catalyzed alkene hydration.
Draw curved arrows to show the movement of electrons in this
step of the reaction mechanism.
Name the following alkene. ball & stick + labels (Include E/Z designations in your names if appropriate. Omit customary italics.) 2,4-dimethyl-3-heptene
Name all of the branched alkene isomers, CH12, that contain 2 methyl branches. pt Include E/Z designations in your names if appropriate. Omit customary italics. If there are fewer than 4 possible compounds, leave the appropriate number of fields blank. Isomer 1: 2,3,-dimethyl-2-butene Isomer 2: 2,3-dimethyl-1-butene Isomer 3: 3,3-dimethyl-1-butene Isomer 4: pt pt pt pt pt
Draw the product(s) of the reaction of the alkene below with O3, followed by Zn in acetic acid.
Name the following including the R/S, E/Z designations. 4. CH3 CH3 Hас Draw the complete mechanism for the following E2 reaction, showing all arrows, intermediates, all products, and label the major product. 5. CH3 о CH3 Hас C. H2 CH3
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick labels ball & stick labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. • Use the wedge/hash bond tools to indicate stereochemistry where...
1) Provide the proper IUPAC name for the alkene shown below. CH2=CHCH2CH2CH2CH3 2) Provide the proper IUPAC name for the alkene shown below. 3) Draw an acceptable structure for 4-ethylhept-1-ene. 4) Provide an acceptable name for (CH3)2CHCH-C(CH3)CH2CH3. 5) Provide an acceptable name for (CH3CH2)2CHCH2CH-CH2. 6) Name the compound shown below. 7) Provide the proper IUPAC name for the alkene shown below. 8) Provide the proper IUPAC name for the alkene shown below. 9) Draw an acceptable structure for 4-phenylbut-l-ene. 10)...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
8.1)
8.5)
Give the appropriate IUPAC name for the following structural formula of a halogenated compound. CH3 CI Нас (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis/trans designations only to represent stereochemistry for cyclic compounds. It is not necessary to use italics in writing compound names.) Name: There are five cycloalkanes with the molecular formula C5H10. When treated with chlorine at 300°C, isomer A gives one monochlorination product. Under the same conditions, isomer B...
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.,...
Draw the products of the following reactions, indicating both
regiochemistry and stereochemistry when appropriate.
draw the organic product(s) expected when this compound
undergoes the Simmons-Smith reaction.
Draw the product of the reaction below.
Reaction of 3-methyl-1-butene with
CH3OH in the presence of H2SO4
catalyst yields 2-methoxy-2-methylbutane by a
mechanism analogous to that of acid-catalyzed alkene hydration.
Draw curved arrows to show the movement of electrons in this
step of the reaction mechanism.
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