III. Carbohydrates A. If a reaction will occur, give the product(s) otherwise write no reaction. Also indicate if the reaction is fast or slow. Explain your answer. он HO H- Resorcinol HCI H- HO. 1. HO.
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If a reaction will occur, give the product. Otherwise, no reaction. Also, indicate if the reaction is fast or slow. Explain your answer.
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- This question is from a study guide for O chem. Can you help me break down the problem and help me understand why it has the steriochemistry that it does.Give the main organic product of the reaction in Figure 6. [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] * Your answershow the major product/s
- Complete the next reactions by writing the products, reactives and experimental conditionsBased on reaction 1, determine the configurations of all chiral centers. Reaction 1 and target molecule are included. Please state the answer in clear words along with any pictures/reactions.Can you explain part d please? why do we put ethyl in the beginning? Also in my answer key for part e it's called 2-methylhexan-2-ol
- Fill in the missing reactant, reagent, and products. Indicate sterochemistry if necessary. assume reagents are in excessWhat is the product (from the image below) of the starting material D-glyceraldehyde which will (1) produce aldaric acid upon reacting with HNO3 + H2O, NaOCH2, NH2OH, and (CH3CO)2O + NaOCOCH3 (2) produce tartaric acid upon reacting with HNO3 + H2O, NaOCH3, NH2OH, and (CH3CO)2O + NaOCOCH3Show the Reaction of ROH with SOCl2 ?
- Draw the structure of the major organic product(s) of the reaction. You do not have to consider stereochemistry. All carboxyl and amino groups should be drawn in the neutral form. If no reaction occurs, draw the organic starting material. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.A student was trying to treat an alcohol with PCC and when they took the IR below they wanted to see if the product had formed. What evidence supports the suspicions that the product did form?How do I rearrange this equation to isolate c? a=b(1/c-1/d)