For the questions below please indicate the expected major product for the indicated reaction. Please indicate the major resonance

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∻Solution∻ ‖ 1 ⋮ **Identify the reaction for the bicyclic ketone compound**: The bicyclic compound with two ketone groups will react with borane (":B") in a reduction process. ‖ ‖ 2 ⋮ **Predict the major product for reaction 1**: The borane will reduce the ketone groups to secondary alcohols. The bicyclic compound will have two hydroxyl groups (-OH) where the ketone groups were originally located. ‖ ‖ 3 ⋮ **Identify the reaction for the heterocyclic compound**: The heterocyclic compound with two nitrogen atoms will react with borane. This reaction is less common, but borane can potentially reduce imine or nitrile groups if present. ‖ ‖ 4 ⋮ **Predict the major product for reaction 2**: Without specific details on the functional groups attached to the nitrogen atoms, a general prediction is challenging. However, if reducible groups are present, borane would reduce them to amines. ‖ ‖ 5 ⋮ **Identify the reaction for the thiol-ester compound**: The molecule containing a thiol (SH) group and an ester (OMe) group will react with borane. Borane typically reduces carbonyl compounds, not thiols or esters. ‖ ‖ 6 ⋮ **Predict the major product for reaction 3**: The borane will not react with the thiol or ester group under normal conditions, so no reaction is expected. ‖ ‖ 7 ⋮ **Identify the reaction for the amine-ester compound with borane**: The molecule containing an amine (NH2) group and an ester (OMe) group will react with borane. Borane might reduce the ester to an alcohol if the conditions are suitable. ‖ ‖ 8 ⋮ **Predict the major product for reaction 4**: The borane could reduce the ester group to an alcohol, leaving the amine group untouched. ‖ ‖ 9 ⋮ **Identify the reaction for the amine-ester compound with a proton**: The same molecule as in reaction 4, but reacting with a proton (H⊕), will undergo an acid-base reaction. ‖ ‖ 10 ⋮ **Predict the major product for reaction 5**: The amine group will be protonated, forming an ammonium ion. The ester group will remain unchanged. ‖ ∻1 Answer∻ ⚹ The bicyclic ketone compound will be reduced to a bicyclic diol. ⚹ ∻2 Answer∻ ⚹ The heterocyclic compound's reaction with borane is uncertain without more information on the functional groups. ⚹ ∻3 Answer∻ ⚹ No reaction is expected for the thiol-ester compound with borane. ⚹ ∻4 Answer∻ ⚹ The amine-ester compound will be reduced by borane to form an alcohol from the ester group, while the amine remains unchanged. ⚹ ∻5 Answer∻ ⚹ The amine group in the amine-ester compound will be protonated to form an ammonium ion when reacting with a proton. ⚹ ∻Key Concept∻ ⚹ Borane is a reducing agent that typically reduces carbonyl compounds to alcohols. ⚹ ∻Explanation∻ ⚹ Borane selectively reduces carbonyl groups in organic compounds, converting ketones to secondary alcohols. It does not typically react with esters or thiols under normal conditions. ⚹◊What would be the expected major product when the molecule containing a thiol (SH) group and an ester (OMe) group reacts with borane?⍭ Generate me a similar question◊

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