why is this answer c and how many mature of diastereomers can I have in the product
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why is this answer c and how many mature of diastereomers can I
have in the...
Ciru3 2) H20, dil. aq. HCI QUESTION 10 2 points Which compound below is suitable for...
Ciru3 2) H20, dil. aq. HCI QUESTION 10 2 points Which compound below is suitable for conversion to a Grignard reagent? 0= olog.com OCH3 OH CH, D) ОА What is the nature of the product in the following reaction? 1) LIAIHA | THỰC. a = NOI 2) H20, dil, aq. HCI o mixture of diastereomers meso compound single enantiomer racemic mixture QUESTION 5 2 points We were unable to transcribe this image
the answers i circled are incorrect. can you give me the correct answers and explain why?...
the answers i circled are incorrect. can you give me the
correct answers and explain why?
postural de Pero ss and so Lalash, an walach asymmetric carbon as Ror S. (3) label the How many asymmetric carbon atoms are present in the following compound A) B) 1 D) 3 E) 4 2) Which of the statements below correctly describes an achiral molecule? The molecule has a nonsuperimposable mirror image. B) The molecule exhibits optical activity when it interacts with plane-polarized...
please explain E. Triterpene 32. The reaction of terephthaloyl chloride with ethylene glycol, shown, forms a...
please explain
E. Triterpene 32. The reaction of terephthaloyl chloride with ethylene glycol, shown, forms a 35. Reduction of D-xylose (shown) with sodium borohydride yields a product that is CHO H OH NaBHA HH HOH CH2OH HOOH H20 CI A. polyester B. polyamide C. polyether D. polycarbonate E polyurethane A. a racemic mixture B. a single pure enantiomer C. an equal mixture of two diastereomers D. an unequal mixture of two diastereomers E. a meso compound 33. Which of the...
is my answer right? university or com p any Br H2O Y Mom ??? OH S...
is my answer right?
university or com p any Br H2O Y Mom ??? OH S Port to ă Toth ♡ ♡ Tu Y Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s). If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g....
How can I find the limiting reagent using my results? Product mass: 0.701g Product melting point:...
How can I find the limiting reagent using my results? Product mass: 0.701g Product melting point: 135.5 - 137.0 ºC Mixed melting point/prod and meso hydrobenzoin: 135.0 - 136.5 ºC Mixed melting point/prod and benzoin racemic mixture: 125.0 - 129.5 ºC benzil: 1.002g NaBH4 : 0.2g
the answers i circled are incorrect. can you give me all the correct answers and explain...
the answers i circled are incorrect. can you give me all the
correct answers and explain why?
2) Which of the statements below correctly describes an achiral molecule? A The molecule has a nonsuperimposable mirror image. cule exhibits optical activity when it interacts with plane-polarized light. C) The molecule has an enantiomer. D) The molecule might be a meso form. E) None of the above 3) Predict the specific rotation of the compound shown. CH нс 4 A) It is...
Select the best description of the major product(s) formed from the following reaction. 1. Hg(OAc)2, H20...
Select the best description of the major product(s) formed from the following reaction. 1. Hg(OAc)2, H20 2. NaBH4, NaOH А. а single achiral compound B. a pair of enantiomers С. а D. the R enantiomer E. the S enantiomer pair of diastereomers F. two constitutional isomers E ОА ОВ ос O F Enter Your Answer: D Incorrect Select the correct relationship between the following two structures. A. conformational isomers B constitutional isomers C. diastereomers D. enantiomers E. identical structures Enter...
Please note: This is 1 practice homework organic chemistry question with 4 parts in A-C to...
Please note: This is 1 practice homework organic chemistry
question with 4 parts in A-C to answer!
1. Give full curved arrow pushing for the electrocyclic ring
closure reaction.
2. Indicate if product is achiral, meso compound or racemic.
3. Draw the HOMO of the reactant cation on top of the
structure.
4. To form your ALLOWED product, did the reaction proceed
conrotatary or disrotatory?
If you are unable to answer any of the parts PLEASE leave
question alone for...
3. (a) (35 pts, pts each) Provide All of the organic products for each of the...
3. (a) (35 pts, pts each) Provide All of the organic products for each of the reactions below. If more than one organic product is formed, provide them all and indicate which product is major (where appropriate). Also indicate the stereochemistry (single enantiomer. racemic mixture, meso, etc.) of the products where appropriate. 1 eq HI MeOH heat NaOEt EtOH, heat 1 eq HB +40°C H,SO heat 1. BH; 2. HO, NaOH, H20 NaOme MeOH, heat
9. C (Z-2-hexene d. They are all of equal stability. Choose the most stable alkene among...
9. C (Z-2-hexene d. They are all of equal stability. Choose the most stable alkene among the following a 1-hexene b. (E)-2-hexene 10. What is the relation between an enantiomer's configuration and its specific rotation? (a) Rcompounds usually are dextrorotatory with few exceptions (b) R compounds always are dextrorotatory. (c) There is no relation. (d) R compounds always are levorotatory 11. How many chiral centers are there in tartaric acid, and how many different stereoisomers exist for this acid? он...
Ciru3 2) H20, dil. aq. HCI QUESTION 10 2 points Which compound below is suitable for conversion to a Grignard reagent? 0= olog.com OCH3 OH CH, D) ОА What is the nature of the product in the following reaction? 1) LIAIHA | THỰC. a = NOI 2) H20, dil, aq. HCI o mixture of diastereomers meso compound single enantiomer racemic mixture QUESTION 5 2 points We were unable to transcribe this image
the answers i circled are incorrect. can you give me the
correct answers and explain why?
postural de Pero ss and so Lalash, an walach asymmetric carbon as Ror S. (3) label the How many asymmetric carbon atoms are present in the following compound A) B) 1 D) 3 E) 4 2) Which of the statements below correctly describes an achiral molecule? The molecule has a nonsuperimposable mirror image. B) The molecule exhibits optical activity when it interacts with plane-polarized...
please explain
E. Triterpene 32. The reaction of terephthaloyl chloride with ethylene glycol, shown, forms a 35. Reduction of D-xylose (shown) with sodium borohydride yields a product that is CHO H OH NaBHA HH HOH CH2OH HOOH H20 CI A. polyester B. polyamide C. polyether D. polycarbonate E polyurethane A. a racemic mixture B. a single pure enantiomer C. an equal mixture of two diastereomers D. an unequal mixture of two diastereomers E. a meso compound 33. Which of the...
is my answer right?
university or com p any Br H2O Y Mom ??? OH S Port to ă Toth ♡ ♡ Tu Y Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s). If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g....
the answers i circled are incorrect. can you give me all the
correct answers and explain why?
2) Which of the statements below correctly describes an achiral molecule? A The molecule has a nonsuperimposable mirror image. cule exhibits optical activity when it interacts with plane-polarized light. C) The molecule has an enantiomer. D) The molecule might be a meso form. E) None of the above 3) Predict the specific rotation of the compound shown. CH нс 4 A) It is...
Select the best description of the major product(s) formed from the following reaction. 1. Hg(OAc)2, H20 2. NaBH4, NaOH А. а single achiral compound B. a pair of enantiomers С. а D. the R enantiomer E. the S enantiomer pair of diastereomers F. two constitutional isomers E ОА ОВ ос O F Enter Your Answer: D Incorrect Select the correct relationship between the following two structures. A. conformational isomers B constitutional isomers C. diastereomers D. enantiomers E. identical structures Enter...
Please note: This is 1 practice homework organic chemistry
question with 4 parts in A-C to answer!
1. Give full curved arrow pushing for the electrocyclic ring
closure reaction.
2. Indicate if product is achiral, meso compound or racemic.
3. Draw the HOMO of the reactant cation on top of the
structure.
4. To form your ALLOWED product, did the reaction proceed
conrotatary or disrotatory?
If you are unable to answer any of the parts PLEASE leave
question alone for...
3. (a) (35 pts, pts each) Provide All of the organic products for each of the reactions below. If more than one organic product is formed, provide them all and indicate which product is major (where appropriate). Also indicate the stereochemistry (single enantiomer. racemic mixture, meso, etc.) of the products where appropriate. 1 eq HI MeOH heat NaOEt EtOH, heat 1 eq HB +40°C H,SO heat 1. BH; 2. HO, NaOH, H20 NaOme MeOH, heat
9. C (Z-2-hexene d. They are all of equal stability. Choose the most stable alkene among the following a 1-hexene b. (E)-2-hexene 10. What is the relation between an enantiomer's configuration and its specific rotation? (a) Rcompounds usually are dextrorotatory with few exceptions (b) R compounds always are dextrorotatory. (c) There is no relation. (d) R compounds always are levorotatory 11. How many chiral centers are there in tartaric acid, and how many different stereoisomers exist for this acid? он...
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