Question
Please help!!
11. (9) Compound X (C H14O) is a chiral molecule. When treated with HBr and heat, Compound X reacts to form 2 new products, C
0 0
Add a comment Improve this question Transcribed image text
Answer #1

X: Y: 2: 6 My o GHz - G H 3 BR Unsaturation index 6+1-14 12 = 0 6tr- 12 = 1 6+1-14 0 2 - CM3 b ИВА - CH=CH2 CM3 CH₂ - C- chci

Add a comment
Know the answer?
Add Answer to:
Please help!! 11. (9) Compound X (C H14O) is a chiral molecule. When treated with HBr...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • please show a detailed mechanism from X-Y, X-Z, Z-W. 2. Compound X, with chemical formula C...

    please show a detailed mechanism from X-Y, X-Z, Z-W. 2. Compound X, with chemical formula C Ho, gives 1,3-dimethylcyclopentane when treated with Hz Over Pt. That same compound, when treated with hot and concentrated KMnO, produces carbon dioxide and Y. Compound X reacts with two equivalents of HBr in the presence of a peroxyether to form compound Z, with chemical formula C H2Br2. When pound Z is heated in methanol it yields compound W, among others. (a) (6 pts., 3...

  • Problem #23: When compound X (C,H,Br) is reacted with sodium cyanide (NaCN) forms compound Y (C,H...

    Problem #23: When compound X (C,H,Br) is reacted with sodium cyanide (NaCN) forms compound Y (C,H,N). Compound Y, upon reduction with H over a Ni catalyst, yields compound Z (C,HIN. The 'H NMR spectrum of X gives two signals, a multiplet at δ = 7.3 ppm (5H) and a singlet at δ 4.25 ppm (2H). The 'H NMR spectrum of Y is similar to that of X in that it shows a multiplet at ö-7.3 ppm (5H) and a singlet...

  • 2) Compound X, CsH.Br. does not react with Br2 or under ozonolysis conditions. Upon treatment with...

    2) Compound X, CsH.Br. does not react with Br2 or under ozonolysis conditions. Upon treatment with potassium hydroxide, X gives only one product, Y. CsHs. Unlike X, Y reacts with Bry and reacts with KMnO.. Ozonolysis followed by reduction with Zn/H* of Y gives Z, CHO. Compound X is an achiral molecule, while Y and Z are chiral molecules. a) How many degrees of unsaturation are there in compound X? b) Propose structures for X, Y, and Z that are...

  • Compound E: C7H6O3 Hi, can someone please help me with the following questions? Draw a molecule...

    Compound E: C7H6O3 Hi, can someone please help me with the following questions? Draw a molecule that combines both of the above fragments. Show ALL hydrogen What is the molecular formula of the molecule you just drew? (Use the following format: CXHYOZ, where X, Y, and Z are numbers.) What is the molecular formula of the molecule you just drew? (Use the following format: CXHYOZ, where X, Y, and Z are numbers.) The difference between the formula you just wrote...

  • Please Help. Identifications of Unknown Compound. I need help figuring this out. Please be detailed on...

    Please Help. Identifications of Unknown Compound. I need help figuring this out. Please be detailed on why you think its correct Introduction One of the most important tasks that chemists are faced with is the separation and identification of compounds from mixtures. Gratifyingly, chemists have multiple tools in the quest to identify unknown organic compounds. Infrared spectroscopy is useful for determining functional groups that may exist in a molecule. NMR spectroscopy tells information about the connectivity of C-H bonds, as...

  • Please help me correct the wrong answer. If you could also tell me what I did...

    Please help me correct the wrong answer. If you could also tell me what I did wrong that would be fantastic, thank you! Lopt.) 10/23/2019 7. (15-ptst Propose structures for the following compounds based on the spectral data provided. Please show or explain all work. All IR absorptions above 1500 cm are given. 7a) Molecular formula CiH4O IR peak at 30o0-2850 cm N SP C 1.10 ppm (doublet, 30 integration units) 3.60 ppm (septet, 5 integration units) 1HNMR data: Aa...

  • please need help with all the questions and ASAP, thank you 11. Please predict the principle...

    please need help with all the questions and ASAP, thank you 11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...

  • NMR IR CAN YOU PLEASE ANSWER AS SOON AS POSSIBLE THANK YOU PLEASE EXPLAIN IT IN DETAIL THANK YOU Experimental Data Only report the IR absorptions that provide diagnosis...

    NMR IR CAN YOU PLEASE ANSWER AS SOON AS POSSIBLE THANK YOU PLEASE EXPLAIN IT IN DETAIL THANK YOU Experimental Data Only report the IR absorptions that provide diagnosis for the major functional groups. Copies of your spectra will be included in your lab report with this information written on the spectra. However, the information should also be included in the body of the report in a text format similar to the example given below IR cm1: 1735 (C-o); MS:...

  • 1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...

    1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...

  • please help in all sections asap! The following two drawings are resonance structures of one compound....

    please help in all sections asap! The following two drawings are resonance structures of one compound. a-o But the following two drawings are not resonance structures Not resonance structures They are, in fact, two different compounds. Choose the correct explanation(s). Select all that apply. Benzene does not have three C-C single bond and three C-C double bonds. In fact, all six C-C bonds of the ring have the same bond order and same length. Benzene have three C- single bond...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT