Homework Answers
The concept used to solve this problem is based on stereochemistry of a double bond.
Hydrocarbons are majorly classified in two categories, saturated hydrocarbons and unsaturated hydrocarbons. Unsaturated hydrocarbons contain multiple bonds such as double bond and triple bonds. Hydrocarbons containing double bonds are called alkenes. Alkenes can exist in two isomeric forms which are cis alkenes and trans alkenes.
An alkene is said to be a cis alkene when the highest priority groups attached to the adjacent olefin carbons are present on the same side of the double bond.
There is no cis double bond in the structure.
There are two trans double bonds present in the structure.
In the structure of compound, there are 2 trans double bonds and 0 cis double bonds.
Add Answer to:
Identify the configurations around the double bonds in the compound below. Selected bonds will be highlighted...
Select the double bonds in the cis configuration. If there are no cis double bonds, do...
Select the double bonds in the cis configuration. If there are no cis double bonds, do not select any bonds. Select the double bonds in the trans configuratic Map there are no trans double bonds, do not select any bonds. H сн. H HC CH3 CH3 Н.С. CH3 CH3 CH3 CH3 сна CH2 CH2 HO HO Name the following alkenes using systematic names. H3C CH3 H3C H CH2 CH2 CH3 CH2 H3c1 -CH₂ Br CH2 CHE CH₂ H сн.
Question 10 of 28 > Identify the configurations around the double bonds in the compound. H3C CH2 CH₃ H₃C Answer B...
Question 10 of 28 > Identify the configurations around the double bonds in the compound. H3C CH2 CH₃ H₃C Answer Bank neither trans CLS
Identify the configurations around the double bonds in the compound Н Нас, CHз CHз CH3 Н...
Identify the configurations around the double bonds in the compound Н Нас, CHз CHз CH3 Н Hзс cis trans Н. Answer Bank H neither cis trans CH2 trans НО о
1 & 2) Draw the product to the reaction below. 3) Select the chiral atoms in...
1 & 2) Draw the product to the reaction below.
3) Select the chiral atoms in the aspartame molecule.
Draw the product to the reaction below: + OH CH3 H3C—_—HĆ-CH3 + H3C—CH2-OH 6-CH2-CH3 + H20 Draw the product to the reaction below: H3C-CH2-0 H3C—CH2—C—OH + CH3 H3C—CH2-OH + H20 Aspartame is a popular sugar substitute. It is 150 times sweeter than sucrose so very little is needed to sweeten foods. Identify the chirality center(s), sometimes called chiral carbon atoms, in...
1 points Save Answe QUESTION 2 Give the configuration of the substituents around double bond D...
1 points Save Answe QUESTION 2 Give the configuration of the substituents around double bond D in the structures below: HO-CH2 HO А B CH, CH CH Hic D CH=CH2 SCH CH2 HO CH-CH3 "CH₂ ОАЕ OBZ C. Neither
31. Identify the compounds in the following pair as structural isomers, same compound or different compounds....
31. Identify the compounds in the following pair as structural isomers, same compound or different compounds. (2 marks) by Tisdom and 32. Match the following physical and chemical properties with octane, C8H18, or magnesium sulfate, MgSO4 a. Contains only covalent bonds b. Melts at 1124 °C c. Is insoluble in water d. Is a liquid at room temperature e. Is a strong electrolyte (1 x 5 = 5 marks) 33. Write the IUPAC name(including cis or trans, if needed) for...
Draw a structural formula of the SR configuration of the compound shown below. Draw a structural formula of the SR c...
Draw a structural formula of the SR configuration of the
compound shown below.
Draw a structural formula of the SR configuration of the compound shown below. HO LCH₃ -NHCH, H3C ephedrine • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.
how does the structure on thr bottom left have 2 stereocenters? I see both Carbons in the CH3 being bonded directly...
how does the structure on thr bottom left have 2 stereocenters? I
see both Carbons in the CH3 being bonded directly to a H, -CH2 and
another -CH3. i do not see how there are 4 different groups that
each chiral carbon is attached to
os structures are show cand trans molecules srent sequence of groups ul (CH3) group and les initially, a-CH- ction gives, initially, a aded to four different 1,2-Disubstituted Cyclohexanes Now consider 1,2-dimethylcyclohexane. The cis and trans...
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination...
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HAC CH OH H,SO (aq) hear o H2CD NaOCH.CH CHCH OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 31. 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) HO,
Lab 6- Extraction of Carvone Pre-lab Questions Date: Name: 1. Assign the configurations of the two...
Lab 6- Extraction of Carvone Pre-lab Questions Date: Name: 1. Assign the configurations of the two stereocenters in the compound below. (2 points) NH 9 Ph . HN OH 2. Assign R or S configuration to the following molecules. (6 points) CH Br H "CH3 CI Edits will not be automatically saved. Save now changes Times New... 12B T U A A EE 18. Between the stress of university and your diet consisting entirely of pizza, potato chips, and chocolate...
Select the double bonds in the cis configuration. If there are no cis double bonds, do not select any bonds. Select the double bonds in the trans configuratic Map there are no trans double bonds, do not select any bonds. H сн. H HC CH3 CH3 Н.С. CH3 CH3 CH3 CH3 сна CH2 CH2 HO HO Name the following alkenes using systematic names. H3C CH3 H3C H CH2 CH2 CH3 CH2 H3c1 -CH₂ Br CH2 CHE CH₂ H сн.
Question 10 of 28 > Identify the configurations around the double bonds in the compound. H3C CH2 CH₃ H₃C Answer Bank neither trans CLS
Identify the configurations around the double bonds in the compound Н Нас, CHз CHз CH3 Н Hзс cis trans Н. Answer Bank H neither cis trans CH2 trans НО о
1 & 2) Draw the product to the reaction below.
3) Select the chiral atoms in the aspartame molecule.
Draw the product to the reaction below: + OH CH3 H3C—_—HĆ-CH3 + H3C—CH2-OH 6-CH2-CH3 + H20 Draw the product to the reaction below: H3C-CH2-0 H3C—CH2—C—OH + CH3 H3C—CH2-OH + H20 Aspartame is a popular sugar substitute. It is 150 times sweeter than sucrose so very little is needed to sweeten foods. Identify the chirality center(s), sometimes called chiral carbon atoms, in...
1 points Save Answe QUESTION 2 Give the configuration of the substituents around double bond D in the structures below: HO-CH2 HO А B CH, CH CH Hic D CH=CH2 SCH CH2 HO CH-CH3 "CH₂ ОАЕ OBZ C. Neither
31. Identify the compounds in the following pair as structural isomers, same compound or different compounds. (2 marks) by Tisdom and 32. Match the following physical and chemical properties with octane, C8H18, or magnesium sulfate, MgSO4 a. Contains only covalent bonds b. Melts at 1124 °C c. Is insoluble in water d. Is a liquid at room temperature e. Is a strong electrolyte (1 x 5 = 5 marks) 33. Write the IUPAC name(including cis or trans, if needed) for...
Draw a structural formula of the SR configuration of the
compound shown below.
Draw a structural formula of the SR configuration of the compound shown below. HO LCH₃ -NHCH, H3C ephedrine • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.
how does the structure on thr bottom left have 2 stereocenters? I
see both Carbons in the CH3 being bonded directly to a H, -CH2 and
another -CH3. i do not see how there are 4 different groups that
each chiral carbon is attached to
os structures are show cand trans molecules srent sequence of groups ul (CH3) group and les initially, a-CH- ction gives, initially, a aded to four different 1,2-Disubstituted Cyclohexanes Now consider 1,2-dimethylcyclohexane. The cis and trans...
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HAC CH OH H,SO (aq) hear o H2CD NaOCH.CH CHCH OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 31. 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) HO,
Lab 6- Extraction of Carvone Pre-lab Questions Date: Name: 1. Assign the configurations of the two stereocenters in the compound below. (2 points) NH 9 Ph . HN OH 2. Assign R or S configuration to the following molecules. (6 points) CH Br H "CH3 CI Edits will not be automatically saved. Save now changes Times New... 12B T U A A EE 18. Between the stress of university and your diet consisting entirely of pizza, potato chips, and chocolate...
Most questions answered within 3 hours.
-
On May 1, First Bank perfected a security interest in Debtor’s
inventory. On June 1, Bob...
asked 32 minutes ago -
A new kind of typhoid shot is being developed by a medical
research team. The old...
asked 2 hours ago -
Write a chemical equation for these reactions. (Use
the lowest possible whole number coefficients.) Include
states-of-matter...
asked 4 hours ago -
For each of the Z-scores below, determine two probabilities
(show four three decimal places): (1) the...
asked 4 hours ago -
Oxidative phosphorylation is achieved through chemiosmotic
coupling, which turns chemical energy into osmotic potential energy
that...
asked 7 hours ago -
Hollywood Shoes would like to maintain their cash account at a
minimum level of $64,000, but...
asked 7 hours ago -
Proteins CtrA-P, DnaA, and GcrA behave similarly to what
molecule in the Eukaryotic Cell Cycle?
asked 7 hours ago -
TRUE OR FALSE
In case of a competitive tender procedure, in the request for
quotation, the...
asked 7 hours ago -
I am a little behind please provide some explanation, will
provide thumbs up.
This question considers...
asked 7 hours ago -
Let say the utility function as U(X,Y) = lnX + Y. Show that the
marginal rate...
asked 7 hours ago -
A current of I=8.0A is flowing in a typical extension cord of
length L=3.00m. The cord...
asked 7 hours ago -
1. When balancing the equation H2SO4 (aq) + NaOH (aq) →
Na2SO4(aq) + H2O(aq), would you...
asked 8 hours ago