From the H NMR spectra of product molecule it is seen that there are total four different types of Proton. Again in the starting molecule there was three different types of proton(excluding the proton of X). This observations indicates that extra one type of proton comes on the product from nucleophile. Since, in H NMR spectra there is a broad singlet peak at around 4.5ppm and broad singlet peak mainly for - OH group.
Now, as the starting material cinyains tertiary group. So,
The mechanism of the reaction is SN1
And the product for the given reaction is d(3-methyl-3-pentanol).
The most likely nucleophile for the given reaction is - OH-.
The given reaction most likely included: low temperature.
The best leaving group for the reaction which gives maximum rate is--- e) -OMs
1 of 5 below). Nur Product Spectra other reaction and on Product Spectra triplet PPM The...
These 5 questions are all linked together from the same reaction scheme. Could you help explain these with your answer? Use the following reaction scheme and product H NMR to answer 5 different questions (Question 1 of 5 below). Nu: Product Spectra other reaction conditions Product Spectra singlet triplet quartet singlet PPM The mechanism for the reaction is: 1 Product Spectra singlet triplet quartet singlet TAO TO The mechanism for the reaction is: OSN1 O E1 O O E2 O...
Use the first picture to answer the following 5 questions. plz and thank you! Nu: Product Spectra other reaction conditions Product Spectra singlet triplet quartet singlet PPM The mechanism for the reaction is: O E2 O E1cb o E1 O SN1 OSN2 Mert PPM The product for the reaction above is: ОН Ob D C The most likely nucleophile for the above reaction is: O CH3OH окоtBu O NaOEt оон ОН,0 The above reaction most likely included: O Polar Aprotic...
HELP PLS For the following HINMR spectra, what is the most likely compound? singlet triplet triplet singlet doublet doublet PPM Give the most appropriate major product for the following E1 reaction: CH3OH ?? ? со ауа
or esterfication for D Which method would give this ketone? CH,CHE 1. PhMgBr 2. H307 1. CH3CH MgBr 2. Hz0+ 1. CH2CHCN 2. PHCN CH3CH,COCI, AICI: TOLONIA O2 and 3 only 1 and 3 only 1. NaCN 2. H30, Heat CONH2 COH со,Н NH2 Question 14 (1 point) Which structure is consistent with the following proton NMR data: 1.2 (3H, triplet, J = 8Hz), 3.7 (2H, quartet, J = 8Hz), 4.1 (2H, singlet), 11.1 (1H, singlet) CH2CH3 och Por o...
What is the splitting and integration for the protons indicated below? triplet, 2H multiplet (5), 1H singlet, 1H doublet, 1H triplet, 1H NH2 OOO The integration on a 'H NMR spectra containing three peaks is as follows for a molecule with the molecular formula C6H12O; A = 18, B = 12, and C = 6.0. How many hydrogens does peak B represent? OB = 12 B = 2 B = 6 B = 6.0 B=4 Draw the structure for 2,4Z-2-bromo-4-ethyl-2,4-hexandiene....
QUESTION 1 Any reaction involving a carbonyl group and a strong acid begins with the same first step, which is __________________ of the carbonyl oxygen. QUESTION 2 Using condensed molecular formulas (C#H#X#Y#) for your answers, predict the products of the reactions of C6H5CH2CHO (phenylacetaldehyde) with these reagents, and identify the functional group produced in the product. Note that the Tx symbol above allows you to do a subscript. a. NaBH4 / CH3OH b. 1. CH3MgBr; 2. H2O c. Ph3P=CHCH3 d....
Question 1 The following reaction between 2-methylbut-2-ene and hydrogen bromide (HBr) is best described as what type of reaction? Refer to the Figure A) Addition B) Substitution C) Elimination D) Rearrangement Question 2 For the reaction in question 1, two products are possible- a major product, and a minor product. For the minor product, what is the splitting pattern for the added hydrogen (highlighted in red) that would be observed in the molecules HINMR spectrum? Refer to the Figure HBr...
Please do 5 and 6 with given spectra FTIR and NMR Spectra After completing a reaction and working up the products, it is still necessary to confirm that the correct product was formed. The most common tools used for this analysis are Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. In the virtual laboratory, 'H and C NMR spectra are available. Details on interpreting FTIR and NMR spectra are found in your textbook. Your instructor may or may...
Using the data provided below. Fill out the tables regarding the FTIR and NMR Spectra for 2-methyl-2-ethoxypropane. FTIR and NMR Spectra After completing a reaction and working up the products, it is still necessary to confirm that the correct product was formed. The most common tools used for this analysis are Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. In the virtual laboratory, 'H and ''C NMR spectra are available. Details on interpreting FTIR and NMR spectra are...
Only need help with 5,6,7 and mechanism FTIR and NMR Spectra After completing a reaction and working up the products, it is still necessary to confirm that the correct product was formed. The most common tools used for this analysis are Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. In the virtual laboratory, 'H and C NMR spectra are available. Details on interpreting FTIR and NMR spectra are found in your textbook. Your instructor may or may not...