please write neatly 1. Draw the products of each of the four steps in the designated...
1. Draw the products of each of the four steps in the designated boxes (5 points per box). step 1 step 2 PCC step 3 2) H20, H step 4 NaOCH, CH, OH Product 2. Draw a detailed mechanism for the transformations shown in: a) Step 2 (5 points): - b) Step 3 (5 points) c) Step 4 (5 points):
Topic: Organic Chemistry Please make all drawings very clear.
Please show all work and side products along with brief
explanations. Thank you.
2. Fill in each box with the expected organic product of the indicated multistep transformation. Be sure that each product you draw takes into account all steps of the transformation, including workup steps! Remember to account for stereochemistry where appropriate. он 1. CrO2, H20 2. MeOH, H+ cat. 1. HNEt2, pyridine 2. LiAlH4, Et20 3. H* workup NMez...
Please answer ALL questions and write clearly/neatly with
explanations. I will give a positive rating.
CEM 352 QUIZ 3: DUE Friday APRIL 3rd before 5:00 PM EST by EMAIL to your TA NAME: ID TA The following quiz contains 4 questions (see next page) and is worth 25 points. You may use your book, lecture notes and internet (but remember - not everything on the internet is true) to find the answers to the questions. There is also a 3...
Please write neatly and if possible steps would be nice.
What are the products of the following reactions? | Cl2 excess a) H2 b) Lindlar catalyst HBr c) excess
steps please
Problem 5 Draw the product of each of the following Grignard Reactions 1) CH3CH MgBr 2) H20 H 1) (CH3)2CHCH2MgBr 2) H2O li OCH, 1) XS CH3MgBr 2) H20
Fill in the boxes over each arrow with the letter that
corresponds to the reagents needed to perform each step of the
multistep synthesis show below. Reagents may be used more than
once, or not at all. Pay close attention to the numbered carbons in
the starting material, and be sure that your answer accounts for
the position of these carbons in the final product.
pts) Fill in the boxes over each arrow with the letter that corresponds to the...
please answer the question
throughly and neatly.
Part B 8 points each write the product formed by the chromic acid Write the acid oxidation of the alcohol below Н. нсон K,Cr, H2SO4, H,0 Write the major products in the o major products in the following reactions 8 points each ONa CH31 OH CH,CCI AICI HIO, OH
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
1) Predict the Products: Using line drawings with proper use of
dashed wedge and solid wedge notation where necessary, draw the
major organic products of the following reactions in the boxes
provided. If no reaction occurs write “no reaction” or “N.R.” in
the box. Include stereochemistry in your answers where appropriate.
If a product is racemic draw both enantiomers or write “racemic”
next to the structure. Assume all reagents written above and below
the arrows are present in excess unless...
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...